Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
0
votes
0
replies
5.9k
views
Comment: C: Markduplicates Creating A Loss Of Mate Pair
9.9 years ago by DG 7.3k
2
votes
0
replies
11k
views
Answer: Answer: pros- and cons- : programming skills vs. GUI
updated 4.6 years ago by 45k • written 10.0 years ago by 7.3k
0
votes
1
reply
11k
views
Comment: Comment: pros- and cons- : programming skills vs. GUI
updated 4.6 years ago by 45k • written 10.0 years ago by 7.3k
0
votes
0
replies
3.3k
views
Comment: C: Hardware spec for exome sequencing?
10.0 years ago by DG 7.3k
0
votes
0
replies
3.3k
views
Comment: C: Hardware spec for exome sequencing?
10.0 years ago by DG 7.3k
1
vote
0
replies
13k
views
Comment: Comment: Do bioinformaticians often break molecular biologists' hearts by being the first
updated 2.6 years ago by 45k • written 10.0 years ago by 7.3k
4
votes
0
replies
13k
views
Answer: Answer: Do bioinformaticians often break molecular biologists' hearts by being the first
updated 2.6 years ago by 45k • written 10.0 years ago by 7.3k
1
vote
0
replies
2.7k
views
Answer: Answer: Tutorials for families of cancer patients
updated 3.3 years ago by 45k • written 10.0 years ago by 7.3k
0
votes
1
reply
4.6k
views
Comment: C: Bowtie multi-threads and SSD vs spindle disk performance
10.0 years ago by DG 7.3k
0
votes
0
replies
9.3k
views
Comment: C: Identifying FLT3-ITD with Pindel
10.0 years ago by DG 7.3k
0
votes
1
reply
5.7k
views
Comment: C: How do you define inter-disciplinary communication, how important are these skil
10.1 years ago by DG 7.3k
0
votes
1
reply
6.0k
views
Answer: A: Should I use Illumina or Ion Torrent for producing data intended for genome rese
10.1 years ago by DG 7.3k
0
votes
0
replies
1.9k
views
Answer: A: Minimum number of samples required for RNA sequencing in a rare disease to prove
10.1 years ago by DG 7.3k
0
votes
0
replies
9.3k
views
Comment: Comment: Identifying FLT3-ITD with Pindel
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
0
votes
1
reply
9.3k
views
Comment: C: Identifying FLT3-ITD with Pindel
10.1 years ago by DG 7.3k
0
votes
0
replies
5.3k
views
Comment: Comment: For the general public seeking advice from this community
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
0
votes
0
replies
5.3k
views
Comment: Comment: For the general public seeking advice from this community
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
5
votes
0
replies
5.3k
views
Answer: Answer: For the general public seeking advice from this community
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
0
votes
0
replies
2.4k
views
Comment: C: What is the best bibliographic database for biomedical text mining?
10.1 years ago by DG 7.3k
1
vote
0
replies
28k
views
Answer: Answer: The difference between Copy Number Alterations, Copy Number Aberrations (CNAs) a
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
0
votes
1
reply
2.4k
views
Answer: Answer: What is the best bibliographic database for biomedical text mining?
updated 3.2 years ago by 45k • written 10.1 years ago by 7.3k
1
vote
2
replies
2.4k
views
Answer: A: published cancer RNAseq data Re-analysis
10.2 years ago by DG 7.3k
0
votes
0
replies
9.3k
views
Comment: Comment: Identifying FLT3-ITD with Pindel
updated 3.2 years ago by 45k • written 10.2 years ago by 7.3k
1
vote
0
replies
4.0k
views
Answer: Answer: Find Rare SNPs (dbSNP/clinVar)
updated 3.2 years ago by 45k • written 10.2 years ago by 7.3k
0
votes
0
replies
4.0k
views
Comment: Comment: Find Rare SNPs (dbSNP/clinVar)
updated 3.2 years ago by 45k • written 10.2 years ago by 7.3k
1
vote
0
replies
12k
views
Comment: C: New features and bug fixes for Biostar to work on during Google Summer of Code
10.2 years ago by DG 7.3k
0
votes
0
replies
2.6k
views
Comment: C: Blast+ standalone : database creation , install BLAST+ locally
10.2 years ago by DG 7.3k
0
votes
1
reply
9.6k
views
Answer: A: How to generate a scale for a phylogenetic tree?
10.2 years ago by DG 7.3k
0
votes
1
reply
4.0k
views
Comment: C: Find Rare SNPs (dbSNP/clinVar)
10.2 years ago by DG 7.3k
0
votes
1
reply
9.1k
views
Comment: C: How to annotate coding and long non-coding RNA together using transcriptome data
10.2 years ago by DG 7.3k
0
votes
1
reply
9.1k
views
Comment: C: How to annotate coding and long non-coding RNA together using transcriptome data
10.2 years ago by DG 7.3k
2
votes
1
reply
9.1k
views
Answer: Answer: How to annotate coding and long non-coding RNA together using transcriptome data
updated 3.2 years ago by 45k • written 10.2 years ago by 7.3k
0
votes
0
replies
3.0k
views
Answer: Answer: SnpSift annotate reporting extra alleles not present in the input VCF
updated 2.9 years ago by 45k • written 10.2 years ago by 7.3k
0
votes
0
replies
2.6k
views
Comment: Comment: computer specs for open-source tools
updated 3.1 years ago by 45k • written 10.2 years ago by 7.3k
1
vote
1
reply
2.6k
views
Answer: Answer: computer specs for open-source tools
updated 3.1 years ago by 45k • written 10.2 years ago by 7.3k
0
votes
0
replies
7.0k
views
Comment: C: Retrieve statistical information from a vcf file using VCF tools
10.2 years ago by DG 7.3k
1
vote
1
reply
7.0k
views
Answer: Answer: Retrieve statistical information from a vcf file using VCF tools
updated 3.1 years ago by 45k • written 10.2 years ago by 7.3k
1
vote
0
replies
2.0k
views
Answer: Answer: Is there any difference between locus specific database and gene variants databa
updated 3.1 years ago by 45k • written 10.2 years ago by 7.3k
0
votes
0
replies
1.9k
views
Answer: A: Detecting mutations with SNP arrays
10.3 years ago by DG 7.3k
0
votes
0
replies
9.9k
views
Comment: Comment: Calculating Exome Coverage
updated 3.1 years ago by 45k • written 10.3 years ago by 7.3k
2
votes
1
reply
2.3k
views
Answer: Answer: websites about finding genes assiociated with rare-disease which is unreported b
updated 3.1 years ago by 45k • written 10.3 years ago by 7.3k
3
votes
0
replies
2.7k
views
Answer: Answer: Gene Identifiers and Databases
updated 3.1 years ago by 45k • written 10.3 years ago by 7.3k
1
vote
0
replies
2.9k
views
Comment: Comment: how to compare variances with VCF file ?
updated 3.0 years ago by 45k • written 10.3 years ago by 7.3k
0
votes
0
replies
2.4k
views
Answer: A: Sequences number of Orthomcl results (groups.txt) were lower than raw data (fast
10.3 years ago by DG 7.3k
1
vote
0
replies
8.9k
views
Comment: C: get biotype for refseq NM transcripts
10.3 years ago by DG 7.3k
5
votes
1
reply
8.9k
views
Answer: Answer: get biotype for refseq NM transcripts
updated 3.0 years ago by 45k • written 10.3 years ago by 7.3k
1
vote
1
reply
8.9k
views
Comment: C: get biotype for refseq NM transcripts
10.3 years ago by DG 7.3k
2
votes
0
replies
4.8k
views
Comment: C: normalization of NGS results
10.3 years ago by DG 7.3k
1
vote
0
replies
2.2k
views
Answer: A: bcbio-nextgen gets stuck indexing fastq's with grabix when using the cancer-drea
10.3 years ago by DG 7.3k
2
votes
0
replies
4.8k
views
Answer: A: normalization of NGS results
10.3 years ago by DG 7.3k
833 results • Page 8 of 17
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