vcf to table
2020年1月7日 — This tool extracts specified fields for each variant in a VCF file to a tab-delimited table, which may be easier to work with than a VCF. By ... ,This package allows one to run basic snpEff annotation on a variant call format VCF file and then convert this output to a wide table. One can use the output to ... ,2017年5月10日 — I want to convert it to sql or csv data format for data modeling in nosql databases such as apache cassandra or mongodb. But before that, I ...,2024年7月31日 — Reads a VCF file and converts to a long format data table. Note, that whilst the data.table object class is very memory efficient, very large ... ,Functions to expand VariantAnnotation CollapsedVCF object and convert to a data frame. ## Author: Sean Davis and Jack Zhu@Meltzerlab, 12/18/2016.,2016年6月8日 — I've tried using both gatk and snpsifts variantotable/extractfields tools, but it will only sum all the INFO counts and not keep them separated.,This tool extracts specified fields for each variant in a VCF file to a tab-delimited table, which may be easier to work with than a VCF. By default, the tool ... ,2019年11月19日 — 1 Answer 1 · It first iterates over SCR_location and stores SNP locations in an associative array seen . · Next it scans modi_VCF and if the 1st ...,2023年10月6日 — What I want is a table with the position, the changes, the number of alleles showing the alteration, read depth at that position, and total # of ...
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vcf to table 相關參考資料
VariantsToTable – GATK - Broad Institute
2020年1月7日 — This tool extracts specified fields for each variant in a VCF file to a tab-delimited table, which may be easier to work with than a VCF. By ... https://gatk.broadinstitute.or freezecodervcfToTable: Convert variant call format to TSV ...
This package allows one to run basic snpEff annotation on a variant call format VCF file and then convert this output to a wide table. One can use the output to ... https://github.com show vcf data in a table
2017年5月10日 — I want to convert it to sql or csv data format for data modeling in nosql databases such as apache cassandra or mongodb. But before that, I ... https://www.biostars.org vcf2DT: VCF file to data table in j-a-thiagenomalicious
2024年7月31日 — Reads a VCF file and converts to a long format data table. Note, that whilst the data.table object class is very memory efficient, very large ... https://rdrr.io Parseconvert a vcf file to tabular format data table ...
Functions to expand VariantAnnotation CollapsedVCF object and convert to a data frame. ## Author: Sean Davis and Jack Zhu@Meltzerlab, 12/18/2016. https://gist.github.com Multisample vcf to table
2016年6月8日 — I've tried using both gatk and snpsifts variantotable/extractfields tools, but it will only sum all the INFO counts and not keep them separated. https://www.biostars.org VariantsToTable (gatk 4.0.1.0 API)
This tool extracts specified fields for each variant in a VCF file to a tab-delimited table, which may be easier to work with than a VCF. By default, the tool ... https://javadoc.io how to pull data from a vcf table
2019年11月19日 — 1 Answer 1 · It first iterates over SCR_location and stores SNP locations in an associative array seen . · Next it scans modi_VCF and if the 1st ... https://stackoverflow.com creating a simple variant analysis table - vcf
2023年10月6日 — What I want is a table with the position, the changes, the number of alleles showing the alteration, read depth at that position, and total # of ... https://help.galaxyproject.org |