From: Petr Danecek Date: Fri, 15 Mar 2013 09:15:51 +0000 (+0000) Subject: Updated man pages X-Git-Url: https://git.donarmstrong.com/?p=samtools.git;a=commitdiff_plain;h=9a8d2b32376f5114962b02125194493803113783 Updated man pages --- diff --git a/samtools.1 b/samtools.1 index 869feaa..5923abd 100644 --- a/samtools.1 +++ b/samtools.1 @@ -1,4 +1,4 @@ -.TH samtools 1 "2 September 2011" "samtools-0.1.18" "Bioinformatics tools" +.TH samtools 1 "15 March 2013" "samtools-0.1.19" "Bioinformatics tools" .SH NAME .PP samtools - Utilities for the Sequence Alignment/Map (SAM) format @@ -981,6 +981,25 @@ tag set to Collecting indel candidates from reads sequenced by an indel-prone technology may affect the performance of indel calling. +Note that there is a new calling model which can be invoked by + + bcftools view -m0.99 ... + +which fixes some severe limitations of the default method. + +For filtering, best results seem to be achieved by first applying the +.IR SnpGap +filter and then applying some machine learning approach + + vcf-annotate -f SnpGap=n + vcf filter ... + +Both can be found in the +.B vcftools +and +.B htslib +package (links below). + .IP o 2 Derive the allele frequency spectrum (AFS) on a list of sites from multiple individuals: @@ -1039,3 +1058,9 @@ specification. .SH SEE ALSO .PP Samtools website: +.br +Samtools latest source: +.br +VCFtools website with stable link to VCF specification: +.br +HTSlib website: