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Alternatives to CNVnator?
copy number variation cnv written 13 months ago by QVINTVS_FABIVS_MAXIMVS2.4k • updated 7 months ago by astulaaa0
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Noisy germline CNV data using CNVKit
cnvkit copy number variation germline cnv gcnv written 17 months ago by omg what am I doing70 • updated 8 months ago by sutturka170
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Recurrent CNV analysis
gistic gene copy number variation cnv written 13 months ago by noshadho10 • updated 13 months ago by Kevin Blighe66k
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copy number variation
copy number variation written 2.4 years ago by v2710 • updated 2.2 years ago by Dattatray Mongad350
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Copy number variation detection
varscan copy number variation snp written 2.4 years ago by v2710 • updated 2.4 years ago by d-cameron2.2k
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Whole Exome data analysis (Hiseq)
variant calling copy number variation rna-seq written 2.7 years ago by prabhakar827910 • updated 2.7 years ago by Sean Davis26k
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Database for Somatic Copy Numbers
database copy number variation written 3.1 years ago by cookersjs20 • updated 3.1 years ago by Max Ivon120
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CNVnator Inputs and Outputs
genome cnvnator copy number variation cnv written 3.5 years ago by styer.alex10 • updated 3.5 years ago by hunter.call130
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How to exclude noisy CNV from study?
dnacopy varscan copy number variation cnv wes written 3.6 years ago by rmateos.110 • updated 3.6 years ago by ivivek_ngs5.0k
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"Copy Number Variation" detection in Tumor only sample
somatic amplicon panel copy number variation written 5.9 years ago by Satish Gupta40 • updated 5.9 years ago by Paul1.4k
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