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comments
0
votes
3
replies
1.7k
views
Comment:
Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
21 months ago by
Chris Miller
22k
4
votes
8
replies
1.7k
views
Modeling RNAseq batch effects using a non-case/control technical replicate
batch-correction
batch-effect
RNA-seq
updated 21 months ago by
jared.andrews07
★ 18k • written 21 months ago by
Chris Miller
22k
0
votes
0
replies
874
views
Answer:
Answer: SciClone R package
22 months ago by
Chris Miller
22k
0
votes
0
replies
843
views
Comment:
Comment: calling somatic variants w/o quality filters
22 months ago by
Chris Miller
22k
1
vote
1
reply
1.1k
views
Answer:
Answer: TCGA - Is vital_status subject to follow_up duration?
2.2 years ago by
Chris Miller
22k
1
vote
0
replies
1.0k
views
Answer:
Answer: Pindel - comparing tumour vs somatic sample
2.6 years ago by
Chris Miller
22k
0
votes
0
replies
1.3k
views
Comment:
Comment: sciclone iteration does not converge
3.0 years ago by
Chris Miller
22k
0
votes
1
reply
1.3k
views
Answer:
Answer: sciclone iteration does not converge
3.0 years ago by
Chris Miller
22k
0
votes
0
replies
4.6k
views
Comment:
Comment: sciClone input vaf file?
3.0 years ago by
Chris Miller
22k
10
votes
1
reply
15k
views
Answer:
A: Problem To Understand Copy-Number Values Per Gene Provided By The Broad Institut
updated 4.2 years ago by
Ram
44k • written 13.1 years ago by
Chris Miller
22k
4
votes
1
reply
27k
views
Comment:
A: Extract Base Based On Position From Bam File
updated 4.2 years ago by
Ram
44k • written 12.4 years ago by
Chris Miller
22k
0
votes
0
replies
1.4k
views
Comment:
C: Effects of applying BQSR twice?
4.4 years ago by
Chris Miller
22k
1
vote
2
replies
1.4k
views
Effects of applying BQSR twice?
bqsr
alignment
qualityscores
sequencing
updated 4.4 years ago by
h.mon
35k • written 4.4 years ago by
Chris Miller
22k
0
votes
0
replies
2.0k
views
Comment:
C: How to distinguish subclone from sciClone or PyClone result
4.6 years ago by
Chris Miller
22k
1
vote
0
replies
2.0k
views
Answer:
A: How to distinguish subclone from sciClone or PyClone result
4.6 years ago by
Chris Miller
22k
1
vote
0
replies
1.2k
views
Answer:
A: Sciclone cluster all around y=x
4.6 years ago by
Chris Miller
22k
0
votes
0
replies
3.0k
views
Answer:
Answer: I have a long list of GI and I want their accession number
updated 2.6 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
0
replies
2.5k
views
Comment:
C: Is there any journal where you can post small programs to solve very specific ta
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
4
votes
0
replies
2.5k
views
Answer:
A: Is there any journal where you can post small programs to solve very specific ta
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
3
votes
1
reply
4.0k
views
Comment:
C: brew - yet another fastq utility
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
1
vote
1
reply
3.1k
views
Answer:
A: bedtools intersect: keep pairing consistent
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
2
votes
0
replies
1.4k
views
Answer:
A: Hot questions in sequencing data accessability
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
1
vote
0
replies
5.7k
views
Comment:
C: align shortreads using R
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
2
votes
1
reply
4.6k
views
Comment:
C: Why do people not call normal and tumor variant separately for somatic mutation
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
6
votes
1
reply
4.6k
views
Answer:
A: Why do people not call normal and tumor variant separately for somatic mutation
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
2
votes
1
reply
3.9k
views
Answer:
A: Why is my ADMIXTURE random seed always 43
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
3
votes
2
replies
4.2k
views
Answer:
A: Reference and dbSNP incompatibility issue (MuTect2)
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
0
replies
3.7k
views
Comment:
C: Generating Read Length?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
2
replies
3.7k
views
Comment:
C: Generating Read Length?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
1
reply
3.7k
views
Answer:
A: Generating Read Length?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
5
votes
1
reply
7.8k
views
Answer:
A: Change chromosome notation to match a new reference
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
17
votes
1
reply
47k
views
Answer:
A: Up-to-date Online RNA Sequence Analysis Training/Courses/Papers?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
0
replies
3.2k
views
Comment:
C: Mixed opinions on somatic variant calling method
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
2
votes
0
replies
3.4k
views
Comment:
C: How can a gene exist on three different chromosomes!?!?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
3
votes
1
reply
3.2k
views
Answer:
A: Mixed opinions on somatic variant calling method
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
1
reply
3.4k
views
Answer:
A: How can a gene exist on three different chromosomes!?!?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
2
votes
1
reply
4.8k
views
Answer:
A: HiSeq vs GA for RNASeqV2 on TCGA
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
0
replies
66k
views
Comment:
C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.9 years ago by
Ram
44k • written 10.5 years ago by
Chris Miller
22k
2
votes
0
replies
3.9k
views
Comment:
C: Calling variants in blood tumor samples without matched normal samples
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
3
votes
0
replies
3.9k
views
Answer:
A: Calling variants in blood tumor samples without matched normal samples
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
0
replies
4.7k
views
Comment:
C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated 4.9 years ago by
Ram
44k • written 10.5 years ago by
Chris Miller
22k
0
votes
1
reply
4.7k
views
Answer:
A: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated 4.9 years ago by
Ram
44k • written 10.5 years ago by
Chris Miller
22k
1
vote
1
reply
4.5k
views
Answer:
C: tbl2asn Permission denied on Mac
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
Chris Miller
22k
2
votes
1
reply
2.7k
views
Answer:
A: Is it correct to merge TCGA mutation data from multiple centers
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
1
reply
3.7k
views
Answer:
A: Somatic allele frequency from TCGA in non-coding DNA
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
0
votes
1
reply
2.5k
views
Answer:
A: Pathway enrichment for Copy Number Alterations (CNA)
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
Chris Miller
22k
3
votes
0
replies
3.6k
views
Answer:
A: What is a repetitive region?
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
Chris Miller
22k
2
votes
0
replies
3.2k
views
Answer:
A: Spliting a dataframe based in a chromosome
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
Chris Miller
22k
0
votes
0
replies
14k
views
Comment:
C: CNV analysis tool on exome data for NGS
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
Chris Miller
22k
0
votes
1
reply
1.7k
views
Comment:
C: SubcloneSeeker SNP import from flat file
updated 4.9 years ago by
Ram
44k • written 8.9 years ago by
Chris Miller
22k
1,036 results • Page
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