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Somatic Structure Variation on exome-seq data - pipeline recommendations?
gatk exome-seq written 12 weeks ago by wiki970 • updated 12 weeks ago by Pierre Lindenbaum132k
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Correlation between coverage and variant calling
exome-seq variant_calling snp written 11 months ago by vinayjrao200 • updated 11 months ago by harish320
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Detecting copy number variants from whole-exome sequencing data
exome-seq cnv written 14 months ago by Shicheng Guo8.5k • updated 14 months ago by hafiz.talhamalik250
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When to remove duplicates using deduplication in Exome-Seq
trueseq dna-seq exome-seq truseq gatk written 2.0 years ago by oriolebaltimore160 • updated 2.0 years ago by Charles Warden8.0k
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[solved] SnpEff reports intron variants in exons ?
annotation snpeff exome-seq snp written 3.3 years ago by δΉ™180 • updated 3.3 years ago by cpad011214k
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converting Indel Realigned Bam to fastq
next-gen exome-seq written 4.0 years ago by IP710 • updated 4.0 years ago by igor12k
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frequently found false positives from exome seq
targetted-capture exome-seq written 6.4 years ago by poisonAlien3.0k • updated 4.2 years ago by Biostar ♦♦ 20
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exome cnv analysis of cases only
case exome-seq cnv written 6.5 years ago by peris120 • updated 6.1 years ago by Vivek Todur50
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cn.mops error - Help !
cn.mops exome-seq r-bioconductor granges written 6.7 years ago by poisonAlien3.0k • updated 6.6 years ago by Biostar ♦♦ 20
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