From 231d3db2635727924ba93d4ab3cff7835471c99b Mon Sep 17 00:00:00 2001 From: ncl935 <33037324+ncl935@users.noreply.github.com> Date: Sun, 30 Aug 2020 18:23:05 +0900 Subject: [PATCH] Update README.md --- README.md | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/README.md b/README.md index 9ef4903..daf762e 100644 --- a/README.md +++ b/README.md @@ -340,7 +340,7 @@ Submodules in __`clair/`__ are for variant calling and model training. Submodule `dataPrepScripts/` | Note: submodules under this folder is Pypy compatiable unless specified. ---: | --- `ExtractVariantCandidates`| Extract the position of variant candidates.
Input: BAM; Reference FASTA.
_Important option(s):
`--threshold` "Minimum alternative allele frequency to report a candidate"
`--minCoverage` "Minimum coverage to report a candidate"_ -`GetTruth`| Extract the variants from a truth VCF. Input: VCF. +`GetTruth`| Extract the variants from a truth VCF. Input: VCF; Reference FASTA if the vcf contains asterisks in ALT field. `CreateTensor`| Create tensors for candidates or truth variants.
Input: A candidate list; BAM; Reference FASTA. `PairWithNonVariants`| Pair truth variant tensors with non-variant tensors.
Input: Truth variants tensors; Candidate variant tensors.
_Important option(s):
`--amp x` "1-time truth variants + x-time non-variants"._ `Tensor2Bin` | Create a compressed binary tensors file to facilitate and speed up future usage.
Input: Mixed tensors by `PairWithNonVariants`; Truth variants by `GetTruth` and a BED file marks the high confidence regions in the reference genome.
(Pypy incompatible)