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CNVkit intervarls questions
cnvkit written 40 minutes ago by emmanouil.a20
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GDC TCGA LUAD dataset iCluster.group parameter
tcgabiolinks R icluster tcga dataset written 18 hours ago by up2015050920 • updated 1 hour ago by igor11k
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Calculating minor allele frequency for GnomAD VCF file
genome gnomad written 3 hours ago by Jamie Watson0 • updated 1 hour ago by Jeremy Leipzig19k
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 4.0 years ago by Istvan Albert ♦♦ 85k • updated 3 hours ago by Shalu Jhanwar470
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How does FastQTL deal with strand
qtl rna-seq written 9 weeks ago by Cindy10 • updated 4 hours ago by Biostar ♦♦ 20
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Find cooccurences of factors across multiple files
gene chip-seq sequencing written 7 hours ago by tirichl20 • updated 6 hours ago by jordi.planells270
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Job: Senior Bioinformatician at Biomage
R next-gen job rna-seq written 6 hours ago by vicky0
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Very large fastq files from RNA-seq
rna-seq sequencing written 11 hours ago by ramyak19120 • updated 6 hours ago by i.sudbery9.7k
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Package to get full Pubmed text in R
R data mining pubmed written 8 hours ago by Bioinformatician_in_trouble10 • updated 6 hours ago by Jean-Karim Heriche23k
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BioMart in R retrieves multiple Entrez IDs for one Ensembl ID
R written 7 hours ago by ali.cham0 • updated 6 hours ago by Kevin Blighe67k
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Why might a large number of variants fail HWE?
genome rna-seq snp written 6 days ago by srmeetd0 • updated 6 hours ago by i.sudbery9.7k
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