Showing: variantsreset
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single sample somatic variant calling software
ffpe somatic tumor pipeline variants written 15 months ago by Zhenyu160 • updated 7 days ago by daniel30
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Getting the variants from EnsEMBL
ensembl genes variants written 12 days ago by keerthuguna960 • updated 12 days ago by Astrid_Ensembl70
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finding directly the snp ids for the variants of each gene
omim dbsnp variants written 13 days ago by jananiinfo140 • updated 13 days ago by Pierre Lindenbaum100k
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Variant Calling in Low-Complexity Regions
indel low-complexity variants snp varscan written 5 weeks ago by ATPoint2.4k • updated 13 days ago by Biostar ♦♦ 20
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Protein coding transcripts with vep
annotation vep variants written 20 months ago by onemoreuser0 • updated 7 weeks ago by Biostar ♦♦ 20
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Interpretation of snpeff results
vcf annotation tool snp variants written 3 months ago by misbahabas40 • updated 9 weeks ago by Pierre Lindenbaum100k
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GATK VariantFiltration invalid expression
filtration gatk ngs variants written 4 months ago by ciemanek20 • updated 4 months ago by finswimmer600
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Using long reads to find a combination of mutations
long reads nanopore snp variants written 4 months ago by eayasi0 • updated 4 months ago by colindaven370
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Disease risk variants from 23andme
variants written 7 months ago by win680
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calling phased variants
phase variants freebayes problem platypus written 20 months ago by mark.rose10 • updated 7 months ago by arezansoff10
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Variants called differ dramatically between runs
vcf variants written 10 months ago by Ram12k • updated 10 months ago by Steven Lakin1.3k
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Other genetic variants representation format besides VCF
vcf variants written 10 months ago by Helene390 • updated 10 months ago by Brian Bushnell14k
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