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Comment: C: Question About Mergesegment.Pl In Varscan 2
updated 4.5 years ago by 43k • written 9.4 years ago by ▴ 40
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Comment: C: pipeline for neo-antigen identification
6.3 years ago by CHANG ▴ 40
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Comment: C: Protocol To Downlad TCGA Data From GDC
7.2 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
8.0 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
8.0 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
8.0 years ago by CHANG ▴ 40
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Comment: Comment: Machine Learning For Prediction of Relapse in Cancer - Part 2 - Building A Rando
updated 18 months ago by 43k • written 8.4 years ago by ▴ 40
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Comment: Comment: workflow for combining multiple microarray studies of same platform
8.6 years ago by CHANG ▴ 40
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2.4k
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Comment: C: workflow for combining multiple microarray studies of same platform
8.6 years ago by CHANG ▴ 40
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6.5k
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Comment: Comment: Absolute/Hapseg on Exome (WES) Data?
updated 2.1 years ago by 43k • written 9.4 years ago by ▴ 40
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Comment: C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
9.4 years ago by CHANG ▴ 40
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Comment: Comment: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
updated 2.2 years ago by 43k • written 9.4 years ago by ▴ 40
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5.2k
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Comment: C: Plotting Cnv Association And Gwas Association In A Single Plot
9.5 years ago by CHANG ▴ 40
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4.9k
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Comment: Comment: RNA seq: tuxedo protocol - separate non-overlapping genes of same XLOC id in cuf
updated 2.3 years ago by 43k • written 9.6 years ago by ▴ 40
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Comment: C: Work With Dnacopy (Bioconductor) And Varscan Copynumber Results
10.1 years ago by CHANG ▴ 40
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