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Comment: C: Question About Mergesegment.Pl In Varscan 2
updated 5.6 years ago by 45k • written 10.5 years ago by ▴ 40
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Comment: C: pipeline for neo-antigen identification
7.3 years ago by CHANG ▴ 40
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Comment: C: Protocol To Downlad TCGA Data From GDC
8.3 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
9.1 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
9.1 years ago by CHANG ▴ 40
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Comment: C: High percentage of UTR mutations in RNAseq
9.1 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 2.6 years ago by 45k • written 9.5 years ago by ▴ 40
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2.8k
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Comment: Comment: workflow for combining multiple microarray studies of same platform
9.7 years ago by CHANG ▴ 40
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2.8k
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Comment: C: workflow for combining multiple microarray studies of same platform
9.7 years ago by CHANG ▴ 40
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Comment: Comment: Absolute/Hapseg on Exome (WES) Data?
updated 3.2 years ago by 45k • written 10.4 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
10.4 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 3.2 years ago by 45k • written 10.5 years ago by ▴ 40
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Comment: C: Plotting Cnv Association And Gwas Association In A Single Plot
10.5 years ago by CHANG ▴ 40
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Comment: Comment: RNA seq: tuxedo protocol - separate non-overlapping genes of same XLOC id in cuf
updated 3.4 years ago by 45k • written 10.7 years ago by ▴ 40
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Comment: C: Work With Dnacopy (Bioconductor) And Varscan Copynumber Results
11.1 years ago by CHANG ▴ 40
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