Showing: variationreset
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Report haplotype frequencies from a region within a phased vcf file
variation haplotype snp written 19 months ago by Krisr460 • updated 4 weeks ago by Biostar ♦♦ 20
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How to Get only one annotation with the SnpEff annotation?
annotation variation snpeff snp written 5 months ago by mhmtgenc8530 • updated 5 months ago by Pierre Lindenbaum115k
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Forum: Theory v Reality
protein forum variation polymorphism dna written 7 months ago by urema0
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7 follow
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How To Retrieve Gene Variations From Ensembl Using The Perl Api?
perl ensembl api variation written 7.8 years ago by Jarretinha3.3k • updated 7 months ago by Biostar ♦♦ 20
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How to retrieve COSMIC variations using Ensembl REST API?
ensembl api variation cosmic written 23 months ago by patrick.durand120 • updated 17 months ago by Biostar ♦♦ 20
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Designating regulatory region threshold
gene ensembl regulation variation promoter written 17 months ago by johntimcham0 • updated 17 months ago by Emily_Ensembl16k
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Forum: Survey for VEP users
ensembl survey variation vep forum written 19 months ago by Emily_Ensembl16k
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How To Tune Parameters When Running Shrimp2 On Longer Illumina Reads
seq variation miseq alignment written 5.9 years ago by kanwarjag910 • updated 21 months ago by Biostar ♦♦ 20
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Bcftools equivalent of vcf-merge R?
vcf variation bcftools genotype written 2.7 years ago by CuriousGuy20 • updated 23 months ago by Biostar ♦♦ 20
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10
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Get number of variations in a huge VCF using Tabix?
vcf tabix variation big data written 3.1 years ago by Dan500 • updated 2.3 years ago by Thomas Johnson70
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chromosomal locations of snps in humvar variant set
variation humvar snp uniprot written 2.7 years ago by arronslacey230 • updated 2.7 years ago by Elisabeth Gasteiger1.5k
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Targeted resequencing analysis workflow
genome assembly next-gen variation written 3.4 years ago by renjukrishna130 • updated 2.7 years ago by ####170
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Is there any existed tool for retrieving DBsnp from Blast output
variation next-gen alignment dbsnp blast written 3.0 years ago by 30977248650 • updated 2.8 years ago by b.nota5.5k
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Genome browser for website (ASP.net)
genome browser variation asp.net snp written 2.9 years ago by Whoknows670 • updated 2.9 years ago by Jean-Karim Heriche17k
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Software For Amova And Population Comparison
population variation written 4.8 years ago by reis.a.rita0 • updated 3.4 years ago by sana.mystudies60
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Illuminia Vs 454 Coverage Spread
illumina variation 454 coverage sequencing written 4.4 years ago by wizard-1410 • updated 4.2 years ago by Biostar ♦♦ 20
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Functional Relevance Of Stop Retained Variants?
genome variation disease functional genomics written 4.7 years ago by Rubal7720 • updated 4.7 years ago by Emily_Ensembl16k
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Low Number Of Replicates Deseq
replicates R variation deseq written 4.8 years ago by federico.gaiti70 • updated 4.8 years ago by Michele Busby1.9k
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Confirming Identified Seq Mutations By Pcr
sequence variation written 4.8 years ago by Raju30 • updated 4.8 years ago by Alex Paciorkowski3.3k
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How To Get Split-Reads From Breakdancer Output
genome variation alignment structural written 4.9 years ago by gundalav260 • updated 4.9 years ago by ernfrid380
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