Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
1
vote
1
reply
5.2k
views
Comment: C: Visualize Gene Fusions
7.6 years ago by Amitm ★ 2.2k
1
vote
1
reply
2.4k
views
Answer: A: Annotation of repeatative elements
7.6 years ago by Amitm ★ 2.2k
0
votes
0
replies
1.9k
views
Comment: C: Un pack cel files
7.6 years ago by Amitm ★ 2.2k
1
vote
0
replies
2.8k
views
Answer: C: Predict if the mutation is activating or deactivating
7.6 years ago by Amitm ★ 2.2k
0
votes
1
reply
7.9k
views
Comment: C: RNA-seq RPKM significance cut off
7.6 years ago by Amitm ★ 2.2k
2
votes
1
reply
7.9k
views
Answer: A: RNA-seq RPKM significance cut off
7.6 years ago by Amitm ★ 2.2k
0
votes
1
reply
1.4k
views
Comment: C: RNAseq assembly for diploid genome.
7.7 years ago by Amitm ★ 2.2k
0
votes
1
reply
2.4k
views
Comment: C: Biology side of bioinformatics
7.7 years ago by Amitm ★ 2.2k
0
votes
0
replies
1.2k
views
Answer: A: bar code manipulation
7.7 years ago by Amitm ★ 2.2k
0
votes
0
replies
983
views
Answer: A: What is the gene corresponding to MIR382 RNA molecule?
7.7 years ago by Amitm ★ 2.2k
2
votes
1
reply
2.2k
views
Comment: C: Cancer RNA-seq data
7.7 years ago by Amitm ★ 2.2k
1
vote
0
replies
4.9k
views
Comment: C: How can I detect lncRNA?
7.7 years ago by Amitm ★ 2.2k
1
vote
0
replies
5.5k
views
Comment: C: dbsnp in vcf format compatible with hg38
7.7 years ago by Amitm ★ 2.2k
2
votes
1
reply
6.1k
views
Comment: C: Which source of annotation files to use, Ensemble or UCSC?
7.7 years ago by Amitm ★ 2.2k
1
vote
2
replies
4.9k
views
Comment: C: How can I detect lncRNA?
7.7 years ago by Amitm ★ 2.2k
1
vote
2
replies
4.9k
views
Comment: C: How can I detect lncRNA?
7.7 years ago by Amitm ★ 2.2k
0
votes
1
reply
4.9k
views
Comment: C: How can I detect lncRNA?
7.7 years ago by Amitm ★ 2.2k
0
votes
1
reply
4.9k
views
Comment: C: How can I detect lncRNA?
7.7 years ago by Amitm ★ 2.2k
0
votes
0
replies
2.6k
views
Comment: C: MuTect --- with more stringent parameter settings I got more mutations -- Is thi
7.8 years ago by Amitm ★ 2.2k
4
votes
2
replies
8.5k
views
Comment: C: From TCGA to GDC (Genomic data commons)
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
1.9k
views
Comment: C: TCGA exons data-de novo isoform assembly
7.8 years ago by Amitm ★ 2.2k
0
votes
0
replies
3.3k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
3.3k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
3.3k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
7.8 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
1.9k
views
Comment: C: TCGA exons data-de novo isoform assembly
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
1.8k
views
Comment: C: getting reads counts at RefSeq genes
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
1.8k
views
Answer: A: getting reads counts at RefSeq genes
7.8 years ago by Amitm ★ 2.2k
1
vote
1
reply
1.9k
views
Comment: C: removing dbsnp for indel vcf
7.9 years ago by Amitm ★ 2.2k
0
votes
0
replies
3.4k
views
Comment: C: Does CDS, start_codon and stop_codon in gtf affect transcriptome assembly by Str
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.4k
views
Comment: C: Does CDS, start_codon and stop_codon in gtf affect transcriptome assembly by Str
7.9 years ago by Amitm ★ 2.2k
4
votes
2
replies
3.4k
views
Answer: A: Does CDS, start_codon and stop_codon in gtf affect transcriptome assembly by Str
7.9 years ago by Amitm ★ 2.2k
0
votes
0
replies
2.2k
views
Comment: C: Few genes with many reads aligned,
7.9 years ago by Amitm ★ 2.2k
1
vote
0
replies
2.2k
views
Comment: C: Few genes with many reads aligned,
7.9 years ago by Amitm ★ 2.2k
1
vote
0
replies
7.0k
views
Comment: C: Picard Markduplicates output
7.9 years ago by Amitm ★ 2.2k
2
votes
1
reply
7.0k
views
Answer: A: Picard Markduplicates output
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Comment: C: Non-cancer somatic mutation calling
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Comment: C: ADTEx coverage issue
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Comment: C: ADTEx coverage issue
7.9 years ago by Amitm ★ 2.2k
0
votes
0
replies
2.6k
views
Comment: C: non human contaminants in sequencing
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Comment: C: ADTEx coverage issue
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.3k
views
Answer: A: ADTEx coverage issue
7.9 years ago by Amitm ★ 2.2k
4
votes
1
reply
3.3k
views
Answer: A: Non-cancer somatic mutation calling
7.9 years ago by Amitm ★ 2.2k
0
votes
1
reply
2.7k
views
Comment: C: High percentage of UTR mutations in RNAseq
8.0 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.0k
views
Comment: C: BLAT: how to select best hit at one genomic position? (queries are repeats)
8.0 years ago by Amitm ★ 2.2k
0
votes
1
reply
3.0k
views
Answer: A: BLAT: how to select best hit at one genomic position? (queries are repeats)
8.0 years ago by Amitm ★ 2.2k
1
vote
1
reply
6.6k
views
Comment: C: New to BEDtools, can't get intersect to work
8.0 years ago by Amitm ★ 2.2k
0
votes
1
reply
2.7k
views
Comment: C: High percentage of UTR mutations in RNAseq
8.0 years ago by Amitm ★ 2.2k
0
votes
3
replies
2.7k
views
Answer: A: High percentage of UTR mutations in RNAseq
8.0 years ago by Amitm ★ 2.2k
1
vote
0
replies
2.3k
views
Comment: C: How to start Gene Analysis?
8.0 years ago by Amitm ★ 2.2k
280 results • Page 4 of 6
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6