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Comment:
C: Question About Mergesegment.Pl In Varscan 2
updated 5.1 years ago by
Ram
44k • written 10.0 years ago by
CHANG
▴ 40
0
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0
replies
2.4k
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Comment:
C: pipeline for neo-antigen identification
6.9 years ago by
CHANG
▴ 40
0
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0
replies
42k
views
Comment:
C: Protocol To Downlad TCGA Data From GDC
7.8 years ago by
CHANG
▴ 40
0
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0
replies
2.9k
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Comment:
C: High percentage of UTR mutations in RNAseq
8.6 years ago by
CHANG
▴ 40
0
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1
reply
2.9k
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Comment:
C: High percentage of UTR mutations in RNAseq
8.6 years ago by
CHANG
▴ 40
0
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0
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2.9k
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Comment:
C: High percentage of UTR mutations in RNAseq
8.6 years ago by
CHANG
▴ 40
0
votes
8
replies
2.9k
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High percentage of UTR mutations in RNAseq
RNA-Seq
updated 8.6 years ago by
Amitm
★ 2.3k • written 8.6 years ago by
CHANG
▴ 40
0
votes
0
replies
68k
views
Comment:
Comment: Machine Learning For Prediction of Relapse in Cancer - Part 2 - Building A Rando
updated 2.2 years ago by
Ram
44k • written 9.0 years ago by
CHANG
▴ 40
1
vote
0
replies
3.8k
views
TCGA RNAseqV2 upper quartile normalization with x1000 adjustment factor
RNA-Seq
updated 2.3 years ago by
Ram
44k • written 9.1 years ago by
CHANG
▴ 40
0
votes
1
reply
2.5k
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Comment:
Comment: workflow for combining multiple microarray studies of same platform
9.2 years ago by
CHANG
▴ 40
0
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0
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2.5k
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Comment:
C: workflow for combining multiple microarray studies of same platform
9.2 years ago by
CHANG
▴ 40
2
votes
4
replies
2.5k
views
workflow for combining multiple microarray studies of same platform
microarray
updated 2.2 years ago by
Ram
44k • written 9.2 years ago by
CHANG
▴ 40
1
vote
1
reply
4.1k
views
Which GRCh37 version to use from snpEff databases for BAMs mapped with GRCh37-lite?
SNP
next-gen
snpeff
updated 2.5 years ago by
Ram
44k • written 9.7 years ago by
CHANG
▴ 40
0
votes
0
replies
6.8k
views
Comment:
Comment: Absolute/Hapseg on Exome (WES) Data?
updated 2.7 years ago by
Ram
44k • written 10.0 years ago by
CHANG
▴ 40
0
votes
2
replies
15k
views
Comment:
C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
10.0 years ago by
CHANG
▴ 40
0
votes
0
replies
15k
views
Comment:
Comment: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
updated 2.8 years ago by
Ram
44k • written 10.0 years ago by
CHANG
▴ 40
0
votes
0
replies
5.5k
views
Comment:
C: Plotting Cnv Association And Gwas Association In A Single Plot
10.1 years ago by
CHANG
▴ 40
11
votes
6
replies
11k
views
identifying miRNA in RNAseq
miRNA
rna-seq
RNA-Seq
mirna
updated 2.9 years ago by
Ram
44k • written 10.2 years ago by
CHANG
▴ 40
1
vote
1
reply
3.1k
views
calling somatic mutations on ion proton data
ion-proton
somatic-mutation
mutect
updated 3.0 years ago by
Ram
44k • written 10.3 years ago by
CHANG
▴ 40
0
votes
1
reply
5.0k
views
Comment:
Comment: RNA seq: tuxedo protocol - separate non-overlapping genes of same XLOC id in cuf
updated 2.9 years ago by
Ram
44k • written 10.2 years ago by
CHANG
▴ 40
1
vote
4
replies
5.0k
views
RNA seq: tuxedo protocol - separate non-overlapping genes of same XLOC id in cuffdiff output
RNA-Seq
updated 2.9 years ago by
Ram
44k • written 10.3 years ago by
CHANG
▴ 40
0
votes
0
replies
9.2k
views
Comment:
C: Work With Dnacopy (Bioconductor) And Varscan Copynumber Results
10.7 years ago by
CHANG
▴ 40
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