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determine exon number from variant genomic coordinates
exome exon variant coordinates human written 9 weeks ago by cocchi.e8980 • updated 9 weeks ago by rbagnall1.6k
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VEP MutationAssessor output
vep mutationassessor variant human written 12 weeks ago by cocchi.e8980 • updated 11 weeks ago by Ben_Ensembl1.5k
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create an haplotype
haplotype variant snp written 11 weeks ago by marmar0
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freebayes haplotype calling (phased variants)
freebayes haplotype phase variant phased written 4.3 years ago by mark.rose40 • updated 12 weeks ago by mikemc10
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List Of Dbsnp Variants Where Reference Genome Has Minor Allele
exome reference dbsnp variant written 8.6 years ago by Ana Rodrigues Grant30 • updated 3 months ago by Biostar ♦♦ 20
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Pipes within VCF INFO Column
vcf exome-sequencing next-gen variant snp written 3 months ago by basay30 • updated 3 months ago by genomax85k
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Why There Are A Lot Of Mq0 Reads In Some Particular Regions?
calling variant written 7.5 years ago by lyz10302012360 • updated 3 months ago by Biostar ♦♦ 20
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Sequence Conflict in Uniprot
variant mutation gwas genomics sequencing written 3 months ago by Negin0 • updated 3 months ago by JC10k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
annotation sequencing variant tool cancer written 4.7 years ago by Collin830 • updated 4 months ago by slcrick230
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Using SnpEff on Galaxy
vcf assembly ngs variant snp written 5 months ago by pmenon09980
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Validating Predictions Of Small Insertions / Deletions
gatk variant written 6.4 years ago by Ron990 • updated 5 months ago by Biostar ♦♦ 20
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few variants annotated with dbSNFP3.5a
vcf sbnsfp dbsnp variant written 6 months ago by Myosotis197910 • updated 6 months ago by RamRS27k
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How to count variant occurrences in .vcf
.vcf ngs variant occurance snp written 16 months ago by darceyc170 • updated 6 months ago by Biostar ♦♦ 20
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Recommendations For Python Vcf Parser/Writer?
vcf python variation variant written 8.5 years ago by Reece270 • updated 7 months ago by Dataman330
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