Skip to content

Commit 7a29abf

Browse files
committed
bumped version
1 parent 8299ac1 commit 7a29abf

2 files changed

Lines changed: 18 additions & 27 deletions

File tree

Changelog.md

Lines changed: 17 additions & 26 deletions
Original file line numberDiff line numberDiff line change
@@ -1,26 +1,17 @@
1-
V 1.2.3 : Adapted to newest sequence-formats. Had to change all the chromosome-related code to the newType Chrom datatype. Also started implementing normaliseBimWithVCF.
2-
3-
V 1.2.4: normaliseBimWithVCF is ready.
4-
5-
V 1.3.0: Lots of refactoring. Lots of testing. Removed some features in vcf2eigenstrat and in pileupCaller, including
6-
the option in pileupCaller to call without a SNP file.
7-
8-
V 1.3.1: Bumped dependency on sequence-formats to new sequence-formats-1.4.0, which includes strand-information in pileup data, as well as
9-
rsIds in freqSum to output the correct rsId, and an option to parse chromosomes X, Y and MT.
10-
11-
V 1.4.0: Added single strand mode, and new triallelic treatment.
12-
13-
V 1.4.0.1: Improved README, fixed output bug in genoStats.hs
14-
15-
V 1.4.0.3: Updated to new sequence-formats version, now including reading of genetic position from eigenstrat files.
16-
17-
V 1.4.0.4:
18-
* Fixed eigenstrat-output in pileupCaller to add a dot after the outputprefix before the file extensions.
19-
* Updated haskell-stack wrapper scripts for EIGENSOFT and ADMIXTOOLS.
20-
* Moved unmaintained scripts into unmaintained folder.
21-
22-
V 1.5.0: Added support for Plink output
23-
24-
V 1.5.1: Added automatic building
25-
26-
V 1.5.2: Fixed a bug with --samplePopName having to be entered after -p or -e. Fixed a bug in the sequence-formats dependency.
1+
# Changelog
2+
3+
- V 1.2.3 : Adapted to newest sequence-formats. Had to change all the chromosome-related code to the newType Chrom datatype. Also started implementing normaliseBimWithVCF.
4+
- V 1.2.4: normaliseBimWithVCF is ready.
5+
- V 1.3.0: Lots of refactoring. Lots of testing. Removed some features in vcf2eigenstrat and in pileupCaller, including
6+
- the option in pileupCaller to call without a SNP file.
7+
- V 1.3.1: Bumped dependency on sequence-formats to new sequence-formats-1.4.0, which includes strand-information in pileup data, as well as rsIds in freqSum to output the correct rsId, and an option to parse chromosomes X, Y and MT.
8+
- V 1.4.0: Added single strand mode, and new triallelic treatment.
9+
- V 1.4.0.1: Improved README, fixed output bug in genoStats.hs
10+
- V 1.4.0.3: Updated to new sequence-formats version, now including reading of genetic position from eigenstrat files.
11+
- V 1.4.0.4:
12+
* Fixed eigenstrat-output in pileupCaller to add a dot after the outputprefix before the file extensions.
13+
* Updated haskell-stack wrapper scripts for EIGENSOFT and ADMIXTOOLS.
14+
* Moved unmaintained scripts into unmaintained folder.
15+
- V 1.5.0: Added support for Plink output
16+
- V 1.5.1: Added automatic building
17+
- V 1.5.2: Fixed a bug with --samplePopName having to be entered after -p or -e. Fixed a bug in the sequence-formats dependency.

sequenceTools.cabal

Lines changed: 1 addition & 1 deletion
Original file line numberDiff line numberDiff line change
@@ -1,5 +1,5 @@
11
name: sequenceTools
2-
version: 1.5.2
2+
version: 1.5.3
33
synopsis: A package with tools for processing DNA sequencing data
44
description: The tools in this package process sequencing Data, in particular from ancient DNA sequencing libraries. Key tool in this package is pileupCaller, a tool to randomly sample genotypes from sequencing data.
55
license: GPL-3

0 commit comments

Comments
 (0)