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Read showing Insertion of 41 bases when aligned with BWA
bowtie2 variant bwa written 3 months ago by kspata70 • updated 3 months ago by swbarnes28.8k
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determine exon number from variant genomic coordinates
exome exon variant coordinates human written 5 months ago by cocchi.e89110 • updated 5 months ago by rbagnall1.7k
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VEP MutationAssessor output
vep mutationassessor variant human written 6 months ago by cocchi.e89110 • updated 6 months ago by Ben_Ensembl1.6k
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create an haplotype
haplotype variant snp written 6 months ago by marmar0
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freebayes haplotype calling (phased variants)
freebayes haplotype phase variant phased written 4.6 years ago by mark.rose40 • updated 6 months ago by mikemc10
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List Of Dbsnp Variants Where Reference Genome Has Minor Allele
exome reference dbsnp variant written 8.9 years ago by Ana Rodrigues Grant30 • updated 6 months ago by Biostar ♦♦ 20
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Pipes within VCF INFO Column
vcf exome-sequencing next-gen variant snp written 7 months ago by basay30 • updated 7 months ago by genomax91k
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Why There Are A Lot Of Mq0 Reads In Some Particular Regions?
calling variant written 7.8 years ago by lyz10302012360 • updated 7 months ago by Biostar ♦♦ 20
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Sequence Conflict in Uniprot
variant mutation gwas genomics sequencing written 7 months ago by Negin0 • updated 7 months ago by JC11k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
annotation sequencing variant tool cancer written 5.0 years ago by Collin850 • updated 7 months ago by slcrick240
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Using SnpEff on Galaxy
vcf assembly ngs variant snp written 8 months ago by pmenon09980
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