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| author | Marius Bakke <mbakke@fastmail.com> | 2020-04-13 20:26:21 +0200 |
|---|---|---|
| committer | Marius Bakke <mbakke@fastmail.com> | 2020-04-13 20:26:21 +0200 |
| commit | fc58cb5bd2f4a4fb9e910f553009fce8a60e56e9 (patch) | |
| tree | 5a69fa6b63a7bfe7232cb98e949912c20775058d /gnu/packages/bioinformatics.scm | |
| parent | 9d89818a359dd0657e4eb7649b29ad4197b8db39 (diff) | |
| parent | bad368b0d794689f3a8a11b58f1ea4987938682e (diff) | |
| download | guix-fc58cb5bd2f4a4fb9e910f553009fce8a60e56e9.tar.gz | |
Merge branch 'master' into core-updates
Diffstat (limited to 'gnu/packages/bioinformatics.scm')
| -rw-r--r-- | gnu/packages/bioinformatics.scm | 4 |
1 files changed, 2 insertions, 2 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm index 4c3d2b793b..cd01027bce 100644 --- a/gnu/packages/bioinformatics.scm +++ b/gnu/packages/bioinformatics.scm @@ -8401,7 +8401,7 @@ system. It is used to analyze experimental crosses for identifying genes contributing to variation in quantitative traits (so-called quantitative trait loci, QTLs). -Using a hidden Markov model, R/qtl allows to estimate genetic maps, to +Using a hidden Markov model, R/qtl estimates genetic maps, to identify genotyping errors, and to perform single-QTL and two-QTL, two-dimensional genome scans.") (license license:gpl3))) @@ -8532,7 +8532,7 @@ of other R packages who wish to make use of HTSlib.") (home-page "https://bioconductor.org/packages/bamsignals") (synopsis "Extract read count signals from bam files") (description - "This package allows to efficiently obtain count vectors from indexed bam + "This package efficiently obtains count vectors from indexed bam files. It counts the number of nucleotide sequence reads in given genomic ranges and it computes reads profiles and coverage profiles. It also handles paired-end data.") |