Showing: variantsreset
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Merge multiple vcf files while preserving FILTER information
vcf merge variants written 5 weeks ago by mkulecka290 • updated 5 weeks ago by Ram13k
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mpileup for PacBio reads
quiver calling pacbio mpileup variants written 9 months ago by Biomonika (Noolean)3.0k • updated 5 weeks ago by tjduncan100
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How do I make a schema with all described variants within a gene?
gene variants schema written 6 weeks ago by spanakorice10 • updated 6 weeks ago by WouterDeCoster25k
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single sample somatic variant calling software
ffpe somatic tumor pipeline variants written 17 months ago by Zhenyu160 • updated 10 weeks ago by daniel30
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Getting the variants from EnsEMBL
ensembl genes variants written 10 weeks ago by keerthuguna960 • updated 10 weeks ago by Astrid_Ensembl70
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finding directly the snp ids for the variants of each gene
omim dbsnp variants written 10 weeks ago by jananiinfo140 • updated 10 weeks ago by Pierre Lindenbaum103k
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Variant Calling in Low-Complexity Regions
indel low-complexity variants snp varscan written 3 months ago by ATPoint2.6k • updated 10 weeks ago by Biostar ♦♦ 20
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Protein coding transcripts with vep
annotation vep variants written 22 months ago by onemoreuser0 • updated 3 months ago by Biostar ♦♦ 20
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Interpretation of snpeff results
vcf annotation tool snp variants written 5 months ago by misbahabas40 • updated 4 months ago by Pierre Lindenbaum103k
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GATK VariantFiltration invalid expression
filtration gatk ngs variants written 6 months ago by ciemanek20 • updated 6 months ago by finswimmer660
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Using long reads to find a combination of mutations
long reads nanopore snp variants written 6 months ago by eayasi0 • updated 6 months ago by colindaven470
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