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how to interpret NES(normalized enrichment score)?
gene R rna-seq written 3 hours ago by ghmdsr0 • updated 1 hour ago by h.mon13k
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Calculate the genotype frequency
vcf ngs written 2 hours ago by SOHAIL170
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111
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Recombination location in gubbins output
genome written 9 weeks ago by mariem.hanachi0 • updated 5 hours ago by Biostar ♦♦ 20
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IGV SNP glyph question
snp igv written 5 hours ago by mark.rose10
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25
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error in star
rna-seq written 7 hours ago by yueli710 • updated 6 hours ago by genomax46k
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16
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22k
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150 follow
16
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 16 months ago by Istvan Albert ♦♦ 76k • updated 6 hours ago by ashakoor0
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63
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pooling reads for error correction
assembly preprocessing error correction rna-seq written 12 hours ago by ilya2390 • updated 8 hours ago by h.mon13k
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120
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Problem with Tophat / Bowtie pipeline
software error rna-seq written 6 days ago by tebb0 • updated 8 hours ago by zx87544.1k
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38
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How to extract the list of genes from TCGA CNV data
tcga genes cnv written 22 hours ago by aouichechaimaa100 • updated 8 hours ago by Kevin Blighe17k
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507
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How to interpret Bayesian network for selected genes
gene bayesian network gene network written 18 months ago by Mike950 • updated 8 hours ago by pfontanarrosa0
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80
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Variant Control Format (VCF) TO Mutation Annotation Format (.MAF)
vcf maf written 1 day ago by genomics Newbie0 • updated 8 hours ago by adam.maikai410
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51
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(Closed) install of STAR
rna-seq written 12 hours ago by yueli710 • updated 9 hours ago by Ram14k
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57
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Nomenclature in HGVS
genome snp written 10 hours ago by mkamranazim0 • updated 9 hours ago by Ram14k
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1
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55
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1
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49
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Count reads from isoforms in RNA-seq data
next-gen isoforms rna-seq splice variants written 11 hours ago by nicanicagm0 • updated 10 hours ago by h.mon13k
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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 7.2 years ago by Jarretinha3.2k • updated 11 hours ago by Biostar ♦♦ 20
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44
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97
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6 follow
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VCF file manipulation for extracting the required information
variant calling vcf file genome sequencing written 14 hours ago by seta960 • updated 12 hours ago by cpad01124.5k
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DESeq2 "Not full rank" Error
deseq2 design written 16 hours ago by Cecelia10 • updated 13 hours ago by swbarnes23.4k
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Combine the fastq files
snp written 13 hours ago by mostafarafiepour0 • updated 13 hours ago by genomax46k
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