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0
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608
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ChIP-nexus peak call
chip-seq written 20 months ago by Sudhir Jadhao50 • updated 2 minutes ago by mlweilert0
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How To Split Vcf Files
vcf vcftools written 1 hour ago by mayara_salvian0 • updated 1 hour ago by Pierre Lindenbaum108k
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Blastn Gives Different Results Based on Database Size
alignment sequence blast written 2 hours ago by khv0 • updated 1 hour ago by lieven.sterck1.6k
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1
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the bam file used for Diffbind
R chip-seq sequencing written 2 hours ago by mikysyc201610 • updated 1 hour ago by jared.andrews07730
352
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16
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24k
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164 follow
16
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 18 months ago by Istvan Albert ♦♦ 77k • updated 1 hour ago by Vijay Lakhujani2.5k
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46
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News: GeNets: a unified web platform for network-based genomic analyses
pathways news visualization networks rna-seq written 3 hours ago by vchris_ngs4.5k • updated 2 hours ago by genomax49k
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50
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DSK: readme and options
gatb written 4 hours ago by sebastien.letort40
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36
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1
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Samtools mpileup returns empty vcf file
samtools mpileup written 3 hours ago by shreyasibiswas8830 • updated 2 hours ago by Ram15k
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drawing comparison gene maps between strains- synterny diagrams
gene software error sequence written 3.4 years ago by mwanerhi erfgtr30 • updated 2 hours ago by Biostar ♦♦ 20
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Remove columns from the VCF file using vcftools
vcftools written 4 hours ago by mayara_salvian0 • updated 4 hours ago by genomax49k
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54
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1
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most sequenced genomes
genomes microbial written 5 hours ago by savscosta0 • updated 4 hours ago by genomax49k
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1
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238
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1
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Classify cells using seurat
monocle scrna seurat written 3 months ago by AB90 • updated 5 hours ago by dppb0540
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28
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10
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211
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9 follow
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Perform of disco Snp with low coverage samples
discosnp snp calling low coverage written 7 days ago by shinken12350 • updated 7 hours ago by pierre.peterlongo760
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7 follow
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3
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48
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How to combine chromosome vcf files
genome assembly next-gen alignment written 7 hours ago by williamsbrian506460 • updated 7 hours ago by Pierre Lindenbaum108k
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1
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106
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