## Release 1.15 (21st February 2022)


* New `bcftools head` subcommand for conveniently displaying the headers
  of a VCF or BCF file. Without any options, this is equivalent to
  `bcftools view --header-only --no-version` but more succinct and memorable.

* The `-T, --targets-file` option had the following bug originating in HTSlib code:
  when an uncompressed file with multiple columns CHR,POS,REF was provided, the
  REF would be interpreted as 0 gigabases (#1598)

Changes affecting specific commands:

* bcftools annotate

    - In addition to `--rename-annots`, which requires a file with name mappings,
      it is now possible to do the same on the command line `-c NEW_TAG:=OLD_TAG`

    - Add new option --min-overlap which allows to specify the minimum required
      overlap of intersecting regions

    - Allow to transfer ALT from VCF with or without replacement using
        bcftools annotate -a annots.vcf.gz -c ALT file.vcf.gz
        bcftools annotate -a annots.vcf.gz -c +ALT file.vcf.gz

* bcftools convert

    - Revamp of `--gensample`, `--hapsample` and `--haplegendsample` family of options
      which includes the following changes:

    - New `--3N6` option to output/input the new version of the .gen file format,
      see https://www.cog-genomics.org/plink/2.0/formats#gen

    - Deprecate the `--chrom` option in favor of `--3N6`. A simple `cut` command
      can be used to convert from the new 3*M+6 column format to the format printed
      with `--chrom` (`cut -d' ' -f1,3-`).

    - The CHROM:POS_REF_ALT IDs which are used to detect strand swaps are required
      and must appear either in the "SNP ID" column or the "rsID" column. The column
      is autodetected for `--gensample2vcf`, can be the first or the second for
      `--hapsample2vcf` (depending on whether the `--vcf-ids` option is given), must be
      the first for `--haplegendsample2vcf`.

* bcftools csq

    - Allow GFF files with phase column unset

* bcftools filter

    - New `--mask`, `--mask-file` and `--mask-overlap` options to soft filter
      variants in regions (#1635)

* bcftools +fixref

    - The `-m id` option now works also for non-dbSNP ids, i.e. not just `rsINT`

    - New `-m flip-all` mode for flipping all sites, including ambiguous A/T and C/G sites

* bcftools isec

    - Prevent segfault on sites filtered with -i/-e in all files (#1632)

* bcftools mpileup

    - More flexible read filtering using the options
        --ls, --skip-all-set    ..  skip reads with all of the FLAG bits set
        --ns, --skip-any-set    ..  skip reads with any of the FLAG bits set
        --lu, --skip-all-unset  ..  skip reads with all of the FLAG bits unset
        --nu, --skip-any-unset  ..  skip reads with any of the FLAG bits unset

      The existing synonymous options will continue to function but their use
      is discouraged
        --rf, --incl-flags STR|INT  Required flags: skip reads with mask bits unset
        --ff, --excl-flags STR|INT  Filter flags: skip reads with mask bits set

* bcftools query

    - Make the `--samples` and `--samples-file` options work also in the `--list-samples`
      mode. Add a new `--force-samples` option which allows to proceed even when some of
      the requested samples are not present in the VCF (#1631)

* bcftools +setGT

    - Fix a bug in `-t q -e EXPR` logic applied on FORMAT fields, sites with all
      samples failing the expression EXPR were incorrectly skipped. This problem
      affected only the use of `-e` logic, not the `-i` expressions (#1607)

* bcftools sort

    - make use of the TMPDIR environment variable when defined

* bcftools +trio-dnm2

    - The --use-NAIVE mode now also adds the de novo allele in FORMAT/VA


## Release 1.14 (22nd October 2021)


Changes affecting the whole of bcftools, or multiple commands:

* New `--regions-overlap` and `--targets-overlap` options which address
  a long-standing design problem with subsetting VCF files by region.
  BCFtools recognize two sets of options, one for streaming (`-t/-T`) and
  one for index-gumping (`-r/-R`). They behave differently, the first
  includes only records with POS coordinate within the regions, the other
  includes overlapping regions. The two new options allow to modify the
  default behavior, see the man page for more details.

* The `--output-type` option can be used to override the default compression
  level

Changes affecting specific commands:

* bcftools annotate

    - when `--set-id` and `--remove` are combined, `--set-id` cannot use
      tags deleted by `--remove`. This is now detected and the program
      exists with an informative error message instead of segfaulting
      (#1540)

    - while non-symbolic variation are uniquely identified by POS,REF,ALT,
      symbolic alleles starting at the same position were undistinguishable.
      This prevented correct matching of records with the same positions and
      variant type but different length given by INFO/END (samtools/htslib@60977f2).
      When annotating froma VCF/BCF, the matching is done automatically. When
      annotating from a tab-delimited text file, this feature can be invoked
      by using `-c INFO/END`.

    - add a new '.' modifier to control wheter missing values should be carried
      over from a tab-delimited file or not. For example:

         -c TAG .. adds TAG if the source value is not missing. If TAG
                   exists in the target file, it will be overwritten

        -c .TAG .. adds TAG even if the source value is missing. This
                   can overwrite non-missing values with a missing value
                   and can create empty VCF fields (`TAG=.`)

* bcftools +check-ploidy

    - by default missing genotypes are not used when determining ploidy.
      With the new option `-m, --use-missing` it is possible to use the
      information carried in the missing and half-missing genotypes
      (e.g. ".", "./." or "./1")

* bcftools concat:

    - new `--ligate-force` and `--ligate-warn` options for finer control
      of `-l, --ligate` behavior in imperfect overlaps. The new default is
      to throw an error when sites present in one chunk but absent in the
      other are encountered. To drop such sites and proceed, use the new
      `--ligate-warn` option (previously this was the default). To keep such
      sites, use the new `--ligate-force` option (#1567).

* bcftools consensus:

    - Apply mask even when the VCF has no notion about the chromosome. It
      was possible to encounter this problem when `contig` lines were not
      present in the VCF header and no variants were called on that chromosome
      (#1592)

* bcftools +contrast:

    - support for chunking within map/reduce framework allowing to collect
      NASSOC counts even for empty case/control sample sets (#1566)

* bcftools csq:

    - bug fix, compound indels were not recognised in some cases (#1536)

    - compound variants were incorrectly marked as 'inframe' even when
      stop codon would occur before the frame was restored (#1551)

    - bug fix, FORMAT/BCSQ bitmasks could have been assigned incorrectly
      to some samples at multiallelic sites, a superset of the correct
      consequences would have been set (#1539)

    - bug fix, the upstream stop could be falsely assigned to all samples in
      a multi-sample VCF even if the stop was relevant for a single sample
      only (#1578)

    - further improve the detection of mismatching chromosome naming
      (e.g. "chrX" vs "X") in the GFF, VCF and fasta files

* bcftools merge:

    - keep (sum) INFO/AN,AC values when merging VCFs with no samples (#1394)

* bcftools mpileup:

    - new --indel-size option which allows to increase the maximum considered
      indel size considered, large deletions in long read data are otherwise
      lost.

* bcftools norm:

    - atomization now supports Number=A,R string annotations (#1503)

    - assign as many alternate alleles to genotypes at multiallelic sites
      in the`-m +` mode, disregarding the phase.  Previously the program
      assumed to be executed as an inverse operation of `-m -`, but when
      that was not the case, reference alleles would have been filled
      instead of multiple alternate alleles (#1542)

* bcftools sort:

    - increase accuracy of the --max-mem option limit, previously the limit
      could be exceeded by more than 20% (#1576)

* bcftools +trio-dnm:

    - new `--with-pAD` option to allow processing of VCFs without FORMAT/QS.
      The existing `--ppl` option was changed to the analogous `--with-pPL`

* bcftools view:

    - the functionality of the option --compression-level lost in 1.12
      has been restored


## Release 1.13 (7th July 2021)


This release brings new options and significant changes in BAQ parametrization
in `bcftools mpileup`. The previous behavior can be triggered by providing
the `--config 1.12` option. Please see https://github.com/samtools/bcftools/pull/1474
for details.


Changes affecting the whole of bcftools, or multiple commands:

* Improved build system


Changes affecting specific commands:

* bcftools annotate:

    - Fix rare a bug when INFO/END is present, all INFO fields are removed
      with `bcftools annotate -x INFO` and BCF output is produced. Then the
      removed INFO/END continues to inform the end coordinate and causes
      incorrect retrieval of records with the -r option (#1483)

    - Support for matching annotation line by ID, in addition to CHROM,POS,REF,
      and ALT (#1461)

        bcftools annotate -a annots.tab.gz  -c CHROM,POS,~ID,REF,ALT,INFO/END input.vcf

* bcftools csq:

    - When GFF and VCF/fasta use a different chromosome naming convention
     (e.g. chrX vs X), no consequences would be added. Newly the program
     attempts to detect these differences and remove/add the "chr" prefix
     to chromosome name to match the GFF and VCF/fasta (#1507)

    - Parametrize brief-predictions parameter to allow explicit number of
      aminoacids to be printed. Note that the `-b, --brief-predictions` option
      is being replaced with `-B, --trim-protein-seq INT`

* bcftools +fill-tags:

    - Generalization and better support for custom functions that allow
      adding new INFO tags based on arbitrary `-i, --include` type of
      expressions. For example, to calculate a missing INFO/DP annotation
      from FORMAT/AD, it is possible to use:

        -t 'DP:1=int(sum(FORMAT/AD))'

      Here the optional ":1" part specifies that a single value will be
      added (by default Number=. is used) and the optional int(...) adds
      an integer value (by default Type=Float is used).

    - When FORMAT/GT is not present, the INFO/AF tag will be newly calculated
      from INFO/AC and INFO/AN.

* bcftools gtcheck:

    - Switch between FORMAT/GT or FORMAT/PL when one is (implicitly) requested
      but only the other is available

    - Improve diagnostics, printing warnings when a line cannot be matched and
      the number of lines skipped for various reasons (#1444)

    - Minor bug fix, with PLs being the default, the `--distinctive-sites` option
      started to require explicit `--error-probability 0`

* bcftools index:

    - The program now accepts both data file name and the index file name. This
      adds to user convenience when running index statistics (-n, -s)

* bcftools isec:

    - Always generate sites.txt with isec -p (#1462)

* bcftools +mendelian:

    - Consider only complete trios, do not crash on sample name typos (#1520)

* bcftools mpileup:

    - New `--seed` option for reproducibility of subsampling code in HTSlib

    - The SCR annotation which shows the number of soft-clipped reads now
      correctly pools reads together regardless of the variant type. Previously
      only reads with indels were included at indel sites.

    - Major revamp of BAQ. Please see https://github.com/samtools/bcftools/pull/1474
      for details. The previous behavior can be triggered by providing the `--config 1.12`
      option.

    - Thanks to improvements in HTSlib, the removal of overlapping reads (which can
      be disabled with the `-x, --ignore-overlaps` options) is not systematically biased
      anymore (https://github.com/samtools/htslib/pull/1273)

    - Modified scale of Mann-Whitney U tests. Newly INFO/*Z annotations will be printed,
      for example MQBZ replaces MQB.

* bcftools norm:

    - Fix Type=Flag output in `norm --atomize` (#1472)

    - Atomization must not discard ALT=. records

    - Atomization of AD and QS tags now correctly updates occurrences of duplicate
      alleles within different haplotypes

    - Fix a bug in atomization of Number=A,R tags

* bcftools reheader:

    - Add `-T, --temp-prefix` option

* bcftools +setGT:

    - A wider range of genotypes can be set by the plugin by allowing
      specifying custom genotypes. For example, to force a heterozygous
      genotype it is now possible to use expressions like:

        c:'m|M'
        c:0/1
        c:0

* bcftools +split-vep:

    - New `-u, --allow-undef-tags` option

    - Better handling of ambiguous keys such as INFO/AF and CSQ/AD. The
      `-p, --annot-prefix` option is now applied before doing anything else
      which allows its use with `-f, --format` and `-c, --columns` options.

    - Some consequence field names may not constitute a valid tag name, such
      as "pos(1-based)". Newly field names are trimmed to exclude brackets.

* bcftools +tag2tag:

    - New --QR-QA-to-QS option to convert annotations generated by Freebays
      to QS used by BCFtools

* bcftools +trio-dnm:

    - Add support for sites with more than four alleles. Note that only the
      four most frequent alleles are considered, the model remains unchanged.
      Previously such sites were skipped.

    - New --use-NAIVE option for a naive DNM calling based solely on FORMAT/GT
      and expected Mendelian inheritance. This option is suitable for prefiltering.

    - Fix behavior to match the documentation, the `--dnm-tag DNG` option now
      correctly outputs log scaled values by default, not phred scaled.

    - Fix bug in VAF calculation, homozygous de novo variants were incorrectly
      reported as having VAF=50%

    - Fix arithmetic underflow which could lead to imprecise scores and improve
      sensitivity in high coverage regions

    - Allow combining --pn and --pns to set the noise trehsholds independently


## Release 1.12 (17th March 2021)

Changes affecting the whole of bcftools, or multiple commands:

* The output file type is determined from the output file name suffix, where
  available, so the -O/--output-type option is often no longer necessary.

* Make F_MISSING in filtering expressions work for sites with multiple
  ALT alleles (#1343)

* Fix N_PASS and F_PASS to behave according to expectation when reverse
  logic is used (#1397). This fix has the side effect of `query` (or
  programs like `+trio-stats`) behaving differently with these expressions,
  operating now in site-oriented rather than sample-oriented mode. For
  example, the new behavior could be:
    bcftools query -f'[%POS %SAMPLE %GT\n]' -i'N_PASS(GT="alt")==1'
        11	A	0/0
        11	B	0/0
        11	C	1/1
  while previously the same expression would return:
        11	C	1/1
  The original mode can be mimicked by splitting the filtering into two steps:
    bcftools view -i'N_PASS(GT="alt")==1' | \
    bcftools query -f'[%POS %SAMPLE %GT\n]' -i'GT="alt"'

Changes affecting specific commands:

* bcftools annotate:

    - New `--rename-annots` option to help fix broken VCFs (#1335)

    - New -C option allows to read a long list of options from a file to
      prevent very long command lines.

    - New `append-missing` logic allows annotations to be added for each ALT
      allele in the same order as they appear in the VCF. Note that this is
      not bullet proof. In order for this to work:

        - the annotation file must have one line per ALT allele

        - fields must contain a single value as multiple values are appended
          as they are and would break the correspondence between the alleles
          and values

* bcftools concat:

    - Do not phase genotypes by mistake if they are not already phased
      with `-l` (#1346)

* bcftools consensus:

    - New `--mask-with`, `--mark-del`, `--mark-ins`, `--mark-snv` options
      (#1382, #1381, #1170)

    - Symbolic <DEL> should have only one REF base. If there are multiple,
      take POS+1 as the first deleted base.

    - Make consensus work when the first base of the reference genome is
      deleted. In this situation the VCF record has POS=1 and the first
      REF base cannot precede the event. (#1330)

* bcftools +contrast:

    - The NOVELGT annotation was previously not added when requested.

* bcftools convert:

    - Make the --hapsample and --hapsample2vcf options consistent with each
      other and with the documentation.

* bcftools call:

    - Revamp of `call -G`, previously sample grouping by population was not
      truly independent and could still be influenced by the presence of other
      sample groups.

    - Optional addition of INFO/PV4 annotation with `call -a INFO/PV4`

    - Remove generation of useless HOB and ICB annotation;
      use `+fill-tags -- -t HWE,ExcHet` instead

    - The `call -f` option was renamed to `-a` to (1) make it consistent with
      `mpileup` and (2) to indicate that it includes both INFO and FORMAT
      annotations, not just FORMAT as previously

    - Any sensible Number=R,Type=Integer annotation can be used with -G,
      such as AD or QS

    - Don't trim QUAL; although usefulness of this change is questionable for
      true probabilistic interpretation (such high precision is unrealistic),
      using QUAL as a score rather than probability is helpful and permits more
      fine-grained filtering

    - Fix a suspected bug in `call -F` in the worst case, for certain improve
      readability

    - `call -C trio` is temporarily disabled

* bcftools csq:

    - Fix a bug wich caused incorrect FORMAT/BCSQ formatting at sites with too
      many per-sample consequences

    - Fix a bug which incorrectly handled the --ncsq parameter and could clash
      with reserved BCF values, consequently producing truncated or even incorrect
      output of the %TBCSQ formatting expression in `bcftools query`. To account
      for the reserved values, the new default value is --ncsq 15 (#1428)

* bcftools +fill-tags:

    - MAF definition revised for multiallelic sites, the second most common
      allele is considered to be the minor allele (#1313)

    - New FORMAT/VAF, VAF1 annotations to set the fraction of alternate reads
      provided FORMAT/AD is present

* bcftools gtcheck:

    - support matching of a single sample against all other samples in the file
      with `-s qry:sample -s gt:-`. This was previously not possible, either
      full cross-check mode had to be run or a list of pairs/samples had to
      be created explicitly

* bcftools merge:

    - Make `merge -R` behavior consistent with other commands and pull in
      overlapping records with POS outside of the regions (#1374)

    - Bug fix (#1353)

* bcftools mpileup:

    - Add new optional tag `mpileup -a FORMAT/QS`

* bcftools norm:

    - New `-a, --atomize` functionality to decompose complex variants,
      for example MNVs into consecutive SNVs

    - New option `--old-rec-tag` to indicate the original variant

* bcftools query:

    - Incorrect fields were printed in the per-sample output when subset
      of samples was requested via -s/-S and the order of samples in the
      header was different from the requested -s/-S order (#1435)

* bcftools +prune:

    - New options --random-seed and --nsites-per-win-mode (#1050)

* bcftools +split-vep:

    - Transcript selection now works also on the raw CSQ/BCSQ annotation.

    - Bug fix, samples were dropped on VCF input and VCF/BCF output (#1349)

* bcftools stats:

    - Changes to QUAL and ts/tv plotting stats: avoid capping QUAL to
      predefined bins, use an open-range logarithmic binning instead

    - plot dual ts/tv stats: per quality bin and cumulative as if threshold
      applied on the whole dataset

* bcftools +trio-dnm2:

    - Major revamp of +trio-dnm plugin, which is now deprecated and replaced by
      +trio-dnm2.

      The original trio-dnm calling model used genotype likelihoods (PLs) as the
      input for calling. However, that is flawed because PLs make assumptions
      which are unsuitable for de novo calling: PL(RR) can become bigger than
      PL(RA) even when the ALT allele is present in the parents. Note that
      this is true also for other programs such as DeNovoGear which rely on
      the same samtools calculation.

      The new recommended workflow is

        bcftools mpileup -a AD,QS -f ref.fa -Ou proband.bam father.bam mother.bam |
           bcftools call -mv -Ou |
           bcftools +trio-dnm -p proband,father,mother -Oz -o output.vcf.gz

      This new version also implements the DeNovoGear model. The original
      behavior of trio-dnm is no longer supported.

      For more details see http://samtools.github.io/bcftools/trio-dnm.pdf


## Release 1.11 (22nd September 2020)


Changes affecting the whole of bcftools, or multiple commands:

* Filtering -i/-e expressions

    - Breaking change in -i/-e expressions on the FILTER column.  Originally
      it was possible to query only a subset of filters, but not an exact match.
      The new behavior is:

        FILTER="A"          .. exact match, for example "A;B" does not pass
        FILTER!="A"         .. exact match, for example "A;B" does pass
        FILTER~"A"          .. both "A" and "A;B" pass
        FILTER!~"A"         .. neither "A" nor "A;B" pass

    - Fix in commutative comparison operators, in some cases reversing sides
      would produce incorrect results (#1224; #1266)

    - Better support for filtering on sample subsests

    - Add SMPL_*/S* family of functions that evaluate within rather than across
      all samples. (#1180)

* Improvements in the build system


Changes affecting specific commands:

* bcftools annotate:

    - Previously it was not possible to use `--columns =TAG` with INFO tags
      and the `--merge-logic` feature was restricted to tab files with BEG,END
      columns, now extended to work also with REF,ALT.

    - Make `annotate -TAG/+TAG` work also with FORMAT fields. (#1259)

    - ID and FILTER can be transferred to INFO and ID can be populated from
      INFO.  However, the FILTER column still cannot be populated from an INFO
      tag because all possible FILTER values must be known at the time of
      writing the header (#947; #1187)

* bcftools consensus:

    - Fix in handling symbolic deletions and overlapping variants.
      (#1149; #1155; #1295)

    - Fix `--iupac-codes` crash on REF-only positions with `ALT="."`. (#1273)

    - Fix `--chain` crash. (#1245)

    - Preserve the case of the genome reference. (#1150)

    - Add new `-a, --absent` option which allows to set positions with no
      supporting evidence to "N" (or any other character). (#848; #940)

* bcftools convert:

    - The option `--vcf-ids` now works also with `-haplegendsample2vcf`. (#1217)

    - New option `--keep-duplicates`

* bcftools csq:

    - Add `misc/gff2gff.py` script for conversion between various flavors of
      GFF files. The initial commit supports only one type and was contributed
      by @flashton2003. (#530)

    - Add missing consequence types. (PR #1203; #1292)

    - Allow overlapping CDS to support ribosomal slippage. (#1208)

* bcftools +fill-tags:

    - Added new annotations: INFO/END, TYPE, F_MISSING.

* bcftools filter:

    - Make `--SnpGap` optionally filter also SNPs close to other variant types.
      (#1126)

* bcftools gtcheck:

    - Complete revamp of the command. The new version is faster and allows
      N:M sample comparisons, not just 1:N or NxN comparisons.
      Some functionality was lost (plotting and clustering) but may be added
      back on popular demand.

* bcftools +mendelian:

    - Revamp of user options, output VCFs with mendelian errors annotation,
      read PED files (thanks to Giulio Genovese).

* bcftools merge:

    - Update headers when appropriate with the '--info-rules *:join' INFO rule.
      (#1282)

    - Local alleles merging that produce LAA and LPL when requested, a draft
      implementation of https://github.com/samtools/hts-specs/pull/434 (#1138)

    - New `--no-index` which allows to merge unindexed files. Requires the input
      files to have chromosomes in th same order and consistent with the order
      of sequences in the header. (PR #1253; samtools/htslib#1089)

    - Fixes in gVCF merging. (#1127; #1164)

* bcftools norm:

    - Fixes in `--check-ref s` reference setting features with non-ACGT bases.
      (#473; #1300)

    - New `--keep-sum` switch to keep vector sum constant when splitting
      multiallelics. (#360)

* bcftools +prune:

    - Extend to allow annotating with various LD metrics: r^2,
      Lewontin's D' (PMID:19433632), or Ragsdale's D (PMID:31697386).

* bcftools query:

    - New `%N_PASS()` formatting expression to output the number of samples
      that pass the filtering expression.

* bcftools reheader:

    - Improved error reporting to prevent user mistakes. (#1288)

* bcftools roh:

    - Several fixes and improvements
        - the `--AF-file` description incorrectly suggested "REF\tALT" instead
          of the correct "REF,ALT". (#1142)
        - RG lines could have negative length. (#1144)
        - new `--include-noalt` option to allow also ALT=. records. (#1137)

* bcftools scatter:

    - New plugin intended as a convenient inverse to `concat`
      (thanks to Giulio Genovese, PR #1249)

* bcftools +split:

    - New `--groups-file` option for more flexibility of defining desired
      output. (#1240)

    - New `--hts-opts` option to reduce required memory by reusing one
      output header and allow overriding the default hFile's block size
      with `--hts-opts block_size=XXX`. On some file systems (lustre) the
      default size can be 4M which becomes a problem when splitting files
      with 10+ samples.

    - Add support for multisample output and sample renaming

* bcftools +split-vep:

    - Add default types (Integer, Float, String) for VEP subfields and make
      `--columns -` extract all subfields into INFO tags in one go.


## Release 1.10.2 (19th December 2019)

This is a release fix that corrects minor inconsistencies discovered in
previous deliverables.


## Release 1.10 (6th December 2019)


* Numerous bug fixes, usability improvements and sanity checks were added
  to prevent common user errors.

* The -r, --regions (and -R, --regions-file) option should never create
  unsorted VCFs or duplicates records again. This also fixes rare cases where
  a spanning deletion makes a subsequent record invisible to `bcftools isec`
  and other commands.

* Additions to filtering and formatting expressions

    - support for the spanning deletion alternate allele (ALT=*)

    - new ILEN filtering expression to be able to filter by indel length

    - new MEAN, MEDIAN, MODE, STDEV, phred filtering functions

    - new formatting expression %PBINOM (phred-scaled binomial probability),
      %INFO (the whole INFO column), %FORMAT (the whole FORMAT column),
      %END (end position of the REF allele), %END0 (0-based end position
      of the REF allele), %MASK (with multiple files indicates the presence
      of the site in other files)

* New plugins

    - `+gvcfz`: compress gVCF file by resizing gVCF blocks according to
      specified criteria

    - `+indel-stats`: collect various indel-specific statistics

    - `+parental-origin`: determine parental origin of a CNV region

    - `+remove-overlaps`: remove overlapping variants.

    - `+split-vep`: query structured annotations such INFO/CSQ created by
      bcftools/csq or VEP

    - `+trio-dnm`: screen variants for possible de-novo mutations in trios

* `annotate`

    - new -l, --merge-logic option for combining multiple overlapping regions

* `call`

    - new `bcftools call -G, --group-samples` option which allows grouping
      samples into populations and applying the HWE assumption within but
      not across the groups.

* `csq`

    - significant reduction of memory usage in the local -l mode for VCFs
      with thousands of samples and 20% reduction in the non-local
      haplotype-aware mode.

    - fixes a small memory leak and formatting issue in FORMAT/BCSQ at
      sites with many consequences

    - do not print protein sequence of start_lost events

    - support for "start_retained" consequence

    - support for symbolic insertions (ALT="<INS...>"), "feature_elongation"
      consequence

    - new -b, --brief-predictions option to output abbreviated protein
      predictions.

* `concat`

    - the `--naive` command now checks header compatibility when concatenating
      multiple files.

* `consensus`

    - add a new `-H, --haplotype 1pIu/2pIu` feature to output first/second
      allele for phased genotypes and the IUPAC code for unphased genotypes

    - new -p, --prefix option to add a prefix to sequence names on output

* `+contrast`

    - added support for Fisher's test probability and other annotations

* `+fill-from-fasta`

    - new -N, --replace-non-ACGTN option

* `+dosage`

    - fix some serious bugs in dosage calculation

* `+fill-tags`

    - extended to perform simple on-the-fly calculations such as calculating
      INFO/DP from FORMAT/DP.

* `merge`

    - add support for merging FORMAT strings

    - bug fixed in gVCF merging

* `mpileup`

    - a new optional SCR annotation for the number of soft-clipped reads

* `reheader`

    - new -f, --fai option for updating contig lines in the VCF header

* `+trio-stats`

    - extend output to include DNM homs and recurrent DNMs

* VariantKey support



## Release 1.9 (18th July 2018)

* `annotate`

    - REF and ALT columns can be now transferred from the annotation file.

    - fixed bug when setting vector_end values.

* `consensus`

    - new -M option to control output at missing genotypes

    - variants immediately following insersions should not be skipped.  Note
      however, that the current fix requires normalized VCF and may still
      falsely skip variants adjacent to multiallelic indels.

    - bug fixed in -H selection handling

* `convert`

    - the --tsv2vcf option now makes the missing genotypes diploid, "./."
      instead of "."

    - the behavior of -i/-e with --gvcf2vcf changed. Previously only sites with
      FILTER set to "PASS" or "." were expanded and the -i/-e options dropped
      sites completely. The new behavior is to let the -i/-e options control
      which records will be expanded. In order to drop records completely,
      one can stream through "bcftools view" first.

* `csq`

    - since the real consequence of start/splice events are not known,
      the amino acid positions at subsequent variants should stay unchanged

    - add `--force` option to skip malformatted transcripts in GFFs with
      out-of-phase CDS exons.

* `+dosage`: output all alleles and all their dosages at multiallelic sites

* `+fixref`: fix serious bug in -m top conversion

* `-i/-e` filtering expressions:

    - add two-tailed binomial test

    - add functions N_PASS() and F_PASS()

    - add support for lists of samples in filtering expressions, with many
      samples it was impractical to list them all on the command line. Samples
      can be now in a file as, e.g., GT[@samples.txt]="het"

    - allow multiple perl functions in the expressions and some bug fixes

    - fix a parsing problem, '@' was not removed from '@filename' expressions

* `mpileup`: fixed bug where, if samples were renamed using the `-G`
  (`--read-groups`) option, some samples could be omitted from the output file.

* `norm`: update INFO/END when normalizing indels

* `+split`: new -S option to subset samples and to use custom file names
  instead of the defaults

* `+smpl-stats`: new plugin

* `+trio-stats`: new plugin

* Fixed build problems with non-functional configure script produced on
  some platforms


## Release 1.8 (April 2018)

* `-i, -e` filtering: Support for custom perl scripts

* `+contrast`: New plugin to annotate genotype differences between groups
  of samples

* `+fixploidy`: New options for simpler ploidy usage

* `+setGT`: Target genotypes can be set to phased by giving `--new-gt p`

* `run-roh.pl`: Allow to pass options directly to `bcftools roh`

* Number of bug fixes


## Release 1.7 (February 2018)

* `-i, -e` filtering: Major revamp, improved filtering by FORMAT fields
  and missing values. New GT=ref,alt,mis etc keywords, check the documentation
  for details.

* `query`: Only matching expression are printed when both the -f and -i/-e
  expressions contain genotype fields. Note that this changes the original
  behavior. Previously all samples were output when one matching sample was
  found. This functionality can be achieved by pre-filtering with view and then
  streaming to query. Compare
        bcftools query -f'[%CHROM:%POS %SAMPLE %GT\n]' -i'GT="alt"' file.bcf
  and
        bcftools view -i'GT="alt"' file.bcf -Ou | bcftools query -f'[%CHROM:%POS %SAMPLE %GT\n]'

* `annotate`: New -k, --keep-sites option

* `consensus`: Fix --iupac-codes output

* `csq`: Homs always considered phased and other fixes

* `norm`: Make `-c none` work and remove `query -c`

* `roh`: Fix errors in the RG output

* `stats`: Allow IUPAC ambiguity codes in the reference file; report the number of missing genotypes

* `+fill-tags`: Add ExcHet annotation

* `+setGt`: Fix bug in binom.test calculation, previously it worked only for nAlt<nRef!

* `+split`: New plugin to split a multi-sample file into single-sample files in one go

* Improve python3 compatibility in plotting scripts



## Release 1.6 (September 2017)

* New `sort` command.

* New options added to the `consensus` command. Note that the `-i, --iupac`
  option has been renamed to `-I, --iupac`, in favor of the standard
  `-i, --include`.

* Filtering expressions (`-i/-e`): support for `GT=<type>` expressions and
  for lists and ranges (#639) - see the man page for details.

* `csq`: relax some GFF3 parsing restrictions to enable using Ensembl
  GFF3 files for plants (#667)

* `stats`: add further documentation to output stats files (#316) and
  include haploid counts in per-sample output (#671).

* `plot-vcfstats`: further fixes for Python3 (@nsoranzo, #645, #666).

* `query` bugfix (#632)

* `+setGT` plugin: new option to set genotypes based on a two-tailed binomial
  distribution test. Also, allow combining `-i/-e` with `-t q`.

* `mpileup`: fix typo (#636)

* `convert --gvcf2vcf` bugfix (#641)

* `+mendelian`: recognize some mendelian inconsistencies that were
  being missed (@oronnavon, #660), also add support for multiallelic
  sites and sex chromosomes.


## Release 1.5 (June 2017)

* Added autoconf support to bcftools. See `INSTALL` for more details.

* `norm`: Make norm case insensitive (#601). Trim the reference allele (#602).

* `mpileup`: fix for misreported indel depths for reads containing adjacent
  indels (3c1205c1).

* `plot-vcfstats`: Open stats file in text mode, not binary (#618).

* `fixref` plugin: Allow multiallelic sites in the `-i, --use-id reference`.
  Also flip genotypes, not just REF/ALT!

* `merge`: fix gVCF merge bug when last record on a chromosome opened a
  gVCF block (#616)

* New options added to the ROH plotting script.

* `consensus`: Properly flush chain info (#606, thanks to @krooijers).

* New `+prune` plugin for pruning sites by LD (R2) or maximum number of
  records within a window.

* New N_MISSING, F_MISSING (number and fraction missing) filtering
  expressions.

* Fix HMM initialization in `roh` when snapshots are used in multiple
  chromosome VCF.

* Fix buffer overflow (#607) in `filter`.


## Release 1.4.1 (8 May 2017)

* `roh`: Fixed malfunctioning options `-m, --genetic-map` and `-M, --rec-rate`,
  and newly allowed their combination. Added a convenience wrapper `misc/run-roh.pl`
  and an interactive script for visualizing the calls `misc/plot-roh.py`.

* `csq`: More control over warning messages (#585).

* Portability improvements (#587). Still work to be done on this front.

* Add support for breakends to `view`, `norm`, `query` and filtering (#592).

* `plot-vcfstats`: Fix for python 2/3 compatibility (#593).

* New `-l, --list` option for `+af-dist` plugin.

* New `-i, --use-id` option for `+fix-ref` plugin.

* Add `--include/--exclude` options to `+guess-ploidy` plugin.

* New `+check-sparsity` plugin.

* Miscellaneous bugfixes for #575, #584, #588, #599, #535.


## Release 1.4 (13 March 2017)

Two new commands - `mpileup` and `csq`:

* The `mpileup` command has been imported from samtools to bcftools. The
  reasoning behind this is that bcftools calling is intimately tied to mpileup
  and any changes to one, often requires changes to the other. Only the
  genotype likelihood (BCF output) part of mpileup has moved to bcftools,
  while the textual pileup output remains in samtools. The BCF output option
  in `samtools mpileup` will likely be removed in a release or two or when
  changes to `bcftools call` are incompatible with the old mpileup output.

  The basic mpileup functionality remains unchanged as do most of the command
  line options, but there are some differences and new features that one
  should be aware of:

  - The option `samtools mpileup -t, --output-tags` changed to `bcftools
    mpileup -a, --annotate` to avoid conflict with the `-t, --targets`
    option common across other bcftools commands.

  - `-O, --output-BP` and `-s, --output-MQ` are no longer used as they are
    only for textual pipelup output, which is not included in `bcftools
    mpileup`. `-O` short option reassigned to `--output-type` and `-s`
    reassigned to `--samples` for consistency with other bcftools commands.

  - `-g, --BCF`, `-v, --VCF`, and ` -u, --uncompressed` options from
    `samtools mpileup` are no longer used, being replaced by the
    `-O, --output-type` option common to other bcftools commands.

  - The `-f, --fasta-ref` option is now required by default to help avoid user
    errors. Can be disabled using `--no-reference`.

  - The option `-d, --depth .. max per-file depth` now behaves as expected
    and according to the documentation, and prints a meaningful diagnostics.

  - The `-S, --samples-file` can be used to rename samples on the fly. See man
    page for details.

  - The `-G, --read-groups` functionality has been extended to allow
    reassignment, grouping and exclusion of readgroups. See man page for
    details.

  - The `-l, --positions` replaced by the `-t, --targets` and
    `-T, --targets-file` options to be consistent with other bcftools
    commands.

  - gVCF output is supported. Per-sample gVCFs created by mpileup can be
    merged using `bcftools merge --gvcf`.

  - Can generate mpileup output on multiple (indexed) regions using the
    `-r, --regions` and `-R, --regions-file` options. In samtools, one
    was restricted to a single region with the `-r, --region` option.

  - Several speedups thanks to @jkbonfield (cf3a55a).

* `csq`: New command for haplotype-aware variant consequence calling.
  See man page and [paper](https://www.ncbi.nlm.nih.gov/pubmed/28205675).


Updates, improvements and bugfixes for many other commands:

* `annotate`: `--collapse` option added. `--mark-sites` now works with
  VCF files rather than just tab-delimited files. Now possible to annotate
  a subset of samples from tab file, not just VCF file (#469). Bugfixes (#428).

* `call`: New option `-F, --prior-freqs` to take advantage of prior knowledge
    of population allele frequencies. Improved calculation of the QUAL score
    particularly for REF sites (#449, 7c56870). `PLs>=256` allowed in
    `call -m`. Bugfixes (#436).

* `concat --naive` now works with vcf.gz in addition to bcf files.

* `consensus`: handle variants overlapping region boundaries (#400).

* `convert`: gvcf2vcf support for mpileup and GATK. new `--sex` option to
  assign sex to be used in certain output types (#500). Large speedup of
  `--hapsample` and `--haplegendsample` (e8e369b) especially with `--threads`
  option enabled. Bugfixes (#460).

* `cnv`: improvements to output (be8b378).

* `filter`: bugfixes (#406).

* `gtcheck`: improved cross-check mode (#441).

* `index` can now specify the path to the output index file. Also, gains the
   `--threads` option.

* `merge`: Large overhaul of `merge` command including support for merging
  gVCF files created by `bcftools mpileup --gvcf` with the new `-g, --gvcf`
  option. New options `-F` to control filter logic and `-0` to set missing
  data to REF. Resolved a number of longstanding issues (#296, #361, #401,
  #408, #412).

* `norm`: Bugfixes (#385,#452,#439), more informative error messages (#364).

* `query`: `%END` plus `%POS0`, `%END0` (0-indexed) support - allows easy BED
  format output (#479). `%TBCSQ` for use with the new `csq` command. Bugfixes
  (#488,#489).

* `plugin`: A number of new plugins:

  - `GTsubset` (thanks to @dlaehnemann)
  - `ad-bias`
  - `af-dist`
  - `fill-from-fasta`
  - `fixref`
  - `guess-ploidy` (deprecates `vcf2sex` plugin)
  - `isecGT`
  - `trio-switch-rate`

  and changes to existing plugins:

  - `tag2tag`: Added `gp-to-gt`, `pl-to-gl` and `--threshold` options and
    bugfixes (#475).
  - `ad-bias`: New `-d` option for minimum depth.
  - `impute-info`: Bugfix (49a9eaf).
  - `fill-tags`:  Added ability to aggregate tags for sample subgroups, thanks
    to @mh11. (#503). HWE tag added as an option.
  - `mendelian`: Bugfix (#566).

* `reheader`: allow muiltispace delimiters in `--samples` option.

* `roh`: Now possible to process multiple samples at once. This allows
  considerable speedups for files with thousands of samples where the cost of
  HMM is neglibible compared to I/O and decompressing. In order to fit tens of
  thousands samples in memory, a sliding HMM can be used (new `--buffer-size`
  option). Viterbi training now uses Baum-Welch algorithm, and works much
  better. Support for gVCFs or FORMAT/PL tags. Added `-o, output` and
  `-O, --output-type` options to control output of sites or regions
  (compression optional). Many bugs fixed - do not segfault on missing PL
  values anymore, a typo in genetic map calculation resulted in a slowdown and
  incorrect results.

* `stats`: Bugfixes (16414e6), new options `-af-bins` and `-af-tags` to control
  allele frequency binning of output. Per-sample genotype concordance tables
  added (#477).

* `view -a, --trim-alt-alleles` various bugfixes for missing data and more
  informative errors should now be given on failure to pinpoint problems.


General changes:

* Timestamps are now added to header lines summarising the command (#467).

* Use of the `--threads` options should be faster across the board thanks to
  changes in HTSlib meaning meaning threads are now shared by the compression
  and decompression calls.

* Changes to genotype filtering with `-i, --include` and `-e, --exclude` (#454).


## Noteworthy changes in release 1.3.1 (22 April 2016)

* The `concat` command has a new `--naive` option for faster operations on
  large BCFs (PR #359).
* `GTisec`: new plugin courtesy of David Laehnemann (@dlaehnemann) to count
  genotype intersections across all possible sample subsets in a VCF file.
* Numerous VCF parsing fixes.
* Build fix: _peakfit.c_ now builds correctly with GSL v2 (#378).
* Various bug fixes and improvements to the `annotate` (#365), `call` (#366),
  `index` (#367), `norm` (#368, #385), `reheader` (#356), and `roh` (#328)
  commands, and to the `fill-tags` (#345) and `tag2tag` (#394) plugins.
* Clarified documentation of `view` filter options, and of the
  `--regions-file` and `--targets-file` options (#357, #411).


## Noteworthy changes in release 1.3 (15 December 2016)

* `bcftools call` has new options `--ploidy` and `--ploidy-file` to make
  handling sample ploidy easier. See man page for details.
* `stats`: `-i`/`-e` short options changed to `-I`/`-E` to be consistent with
  the filtering `-i`/`-e` (`--include`/`--exclude`) options used in other
  tools.
* general `--threads` option to control the number of output compression
  threads used when outputting compressed VCF or BCF.
* `cnv` and `polysomy`: new commands for detecting CNVs, aneuploidy, and
  contamination from SNP genotyping data.
* various new options, plugins, and bug fixes, including #84, #201, #204,
  #205, #208, #211, #222, #225, #242, #243, #249, #282, #285, #289, #302,
  #311, #318, #336, and #338.


## Noteworthy changes in release 1.2 (2 February 2016)

* new `bcftools consensus` command
* new `bcftools annotate` plugins: fixploidy, vcf2sex, tag2tag
* more features in `bcftools convert` command, amongst others new
  `--hapsample` function (thanks to Warren Kretzschmar @wkretzsch)
* support for complements in `bcftools annotate --remove`
* support for `-i`/`-e` filtering expressions in `bcftools isec`
* improved error reporting
* `bcftools call`
  - the default prior increased from `-P 1e-3` to `-P 1.1e-3`, some clear
    calls were missed with default settings previously
  - support for the new symbolic allele `<*>`
  - support for `-f GQ`
  - bug fixes, such as: proper trimming of DPR tag with `-c`; the `-A` switch
    does not add back records removed by `-v` and the behaviour has been made
    consistent with `-c` and `-m`
* many bug fixes and improvements, such as
  - bug in filtering, FMT & INFO vs INFO & FMT
  - fixes in `bcftools merge`
  - filter update AN/AC with `-S`
  - isec outputs matching records for both VCFs in the Venn mode
  - annotate considers alleles when working with `Number=A,R` tags
  - new `--set-id` feature for annotate
  - `convert` can be used similarly to `view`
