Showing: snvreset
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VARIANT effect retrieving
indel variant effect snv written 3 months ago by cocchi.e8930 • updated 7 weeks ago by Biostar ♦♦ 20
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finding out SNPs from SNVs and breed specific SNPs
snv snp written 3 months ago by prasundutta87330 • updated 8 weeks ago by Biostar ♦♦ 20
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Can't find position in GnomAD VCF
vcf snv gnomad written 11 weeks ago by bzg40 • updated 11 weeks ago by zx87547.8k
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Running time in different callers
varscan snv mutect wgs written 11 weeks ago by F3.4k
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New Variants Effect Prediction Tools
indel variant effect snv written 3 months ago by cocchi.e8930 • updated 3 months ago by Emily_Ensembl18k
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TCGA Broad Institute curated variants
broad institute tcga snv rna-seq written 3.2 years ago by umn_bist320 • updated 4 months ago by Biostar ♦♦ 20
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What happens when SNV caller looks at a SV (e.g. deletion) region?
snv deletion written 4 months ago by DVA530 • updated 4 months ago by WouterDeCoster40k
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Using SSrGE for SNV calling
ssrge snv written 5 months ago by landscape95160
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Annotation format for SNVs
snv snp written 8 months ago by Hamid10
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Hard time trying to calculate Allele Frequency and DP from Platypus
snv rna-seq written 19 months ago by simplitia30 • updated 10 months ago by Kevin Blighe45k
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using the docker container of cgpPINDEL
indel wgs snv pindel written 13 months ago by Bogdan800 • updated 12 months ago by Biostar ♦♦ 20
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a realiable algorithm that calls INDELS of length 50bp-300bp in cancer genomes
indel sv snv cnv written 16 months ago by Bogdan800 • updated 16 months ago by Eric T.2.5k
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Tool to identify recurrent mutations directly from VCF
vcf recurrent mutation mutation snv written 22 months ago by ATpoint19k • updated 18 months ago by Biostar ♦♦ 20
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Dataset preparation for driver/passenger gene discovery
gene tcga snv snp cancer written 22 months ago by mhasa00650 • updated 22 months ago by Kevin Blighe45k
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