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Flanking sequence retreival
fasta sequence extraction variants written 5 days ago by nadiabeg.comsats0 • updated 5 days ago by finswimmer13k
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Using dbSNP dataset
vcf dbsnp variants written 7 days ago by rotemkat0
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How to write HGVS nomination for noncoding intergenic variants
genome hgvs snp variants written 27 days ago by hsamireh0 • updated 27 days ago by manuel.belmadani1.2k
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index tabulate file to get chrom, pos, ref, alt
indexing tabix coordinates variants written 5 weeks ago by damian.loska10 • updated 5 weeks ago by Pierre Lindenbaum125k
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Extracting divergence times from 4DTv
substitution variants time 4dtv divergence written 13 months ago by Macspider3.0k • updated 3 months ago by Biostar ♦♦ 20
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Publicly available lymphoma datasets
methylation rna-seq variants written 5 months ago by Stefan0 • updated 5 months ago by jared.andrews074.3k
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Stats on WGS variant calls
wgs variants written 6 months ago by abbysue10 • updated 6 months ago by reza.jabal350
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Applying hard filters for variants
variant calling gatk snps variants written 4.2 years ago by bioinforesearchquestions270 • updated 7 months ago by Biostar ♦♦ 20
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searching tool for calculating switch/phase error rate
vcf variants phasing whatshap written 10 months ago by WouterDeCoster42k • updated 8 months ago by soulsacross60
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Protein coding transcripts with vep
annotation vep variants written 3.9 years ago by onemoreuser10 • updated 8 months ago by abio0
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Lots of alleles in the same place?
alleles snps bcftools variants written 8 months ago by tbb2110 • updated 8 months ago by Kevin Blighe53k
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Pathogenic predictors for Drosophila variants?
genome drosophila variants written 9 months ago by david.rinker10 • updated 8 months ago by Denise - Open Targets5.1k
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