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0
votes
1
reply
3.5k
views
Comment:
C: Problems getting read number per gene after sequencing
8.1 years ago by
trausch
★ 2.0k
0
votes
0
replies
2.6k
views
Answer:
A: Sequence uniformity cov
8.2 years ago by
trausch
★ 2.0k
3
votes
1
reply
6.3k
views
Answer:
A: Program to calculate and add the NM tag to a bam file
8.2 years ago by
trausch
★ 2.0k
4
votes
0
replies
9.0k
views
Answer:
A: Need help : cut the fasta sequences from a specific region
8.2 years ago by
trausch
★ 2.0k
2
votes
0
replies
4.4k
views
Answer:
A: How can I check the direction of DNA replication?
8.2 years ago by
trausch
★ 2.0k
0
votes
0
replies
6.5k
views
Comment:
C: QC for Whole Exome Sequence Data
8.2 years ago by
trausch
★ 2.0k
0
votes
0
replies
3.3k
views
Answer:
A: Structural Variation Discovery: Delly's Output
8.2 years ago by
trausch
★ 2.0k
4
votes
2
replies
3.4k
views
Answer:
A: chromosomal locations of telomeric regions from the Genome
8.2 years ago by
trausch
★ 2.0k
0
votes
1
reply
2.5k
views
Comment:
C: primer design tool suggestions
8.3 years ago by
trausch
★ 2.0k
0
votes
0
replies
3.3k
views
Answer:
A: Help: Phred quality for ab1 files
8.5 years ago by
trausch
★ 2.0k
1
vote
0
replies
2.4k
views
Answer:
A: Full intronic deletions on a Whole-Exome Sequencing experiment
8.6 years ago by
trausch
★ 2.0k
0
votes
0
replies
5.3k
views
Answer:
A: How/where to download Human recombination map/hotspots?
9.0 years ago by
trausch
★ 2.0k
2
votes
1
reply
5.2k
views
Answer:
A: Filter VCF by sample?
9.0 years ago by
trausch
★ 2.0k
0
votes
1
reply
2.9k
views
Comment:
C: Warning from lumpyexpress when calling copy number variants
9.1 years ago by
trausch
★ 2.0k
0
votes
0
replies
3.4k
views
Comment:
C: Estimate stdev and mean in paired-end
9.1 years ago by
trausch
★ 2.0k
0
votes
0
replies
7.5k
views
Comment:
C: Running Delly for structural Variants
9.1 years ago by
trausch
★ 2.0k
0
votes
1
reply
7.5k
views
Comment:
C: Running Delly for structural Variants
9.1 years ago by
trausch
★ 2.0k
2
votes
2
replies
7.5k
views
Answer:
A: Running Delly for structural Variants
9.1 years ago by
trausch
★ 2.0k
0
votes
0
replies
3.4k
views
Comment:
C: Prioritize structural variation (SV) callings supported by multiple softwares
9.4 years ago by
trausch
★ 2.0k
2
votes
1
reply
3.4k
views
Comment:
C: Prioritize structural variation (SV) callings supported by multiple softwares
9.4 years ago by
trausch
★ 2.0k
2
votes
1
reply
4.8k
views
Answer:
A: Cosmic mutation signature
9.6 years ago by
trausch
★ 2.0k
1
vote
0
replies
8.9k
views
Comment:
C: Fastq dump error
9.7 years ago by
trausch
★ 2.0k
2
votes
1
reply
2.9k
views
Comment:
C: check whether two bam files are sequenced from the same sample
9.7 years ago by
trausch
★ 2.0k
1
vote
0
replies
5.0k
views
Answer:
A: How to change snp ID to Variation ID of Clinvar Database
9.7 years ago by
trausch
★ 2.0k
1
vote
0
replies
1.9k
views
Comment:
C: Are there any available genome data files in .AVRO format
9.7 years ago by
trausch
★ 2.0k
3
votes
1
reply
5.7k
views
Answer:
C: shapeIt - prephasing - 1000g genetic map
9.7 years ago by
trausch
★ 2.0k
0
votes
0
replies
3.8k
views
Comment:
C: What could be the reason for having mutations in too many cancer samples?
9.7 years ago by
trausch
★ 2.0k
0
votes
0
replies
1.5k
views
Comment:
C: Can reseq data set with different read lengths generated from Trimmomatic be use
9.7 years ago by
trausch
★ 2.0k
3
votes
1
reply
10.0k
views
Answer:
A: What is the best way to make a bam file smaller by removing unwanted information
9.7 years ago by
trausch
★ 2.0k
2
votes
1
reply
2.7k
views
Answer:
A: GRCh37 database, population filter
9.7 years ago by
trausch
★ 2.0k
0
votes
0
replies
2.7k
views
Answer:
A: checking many somatic mutations in IGV
9.7 years ago by
trausch
★ 2.0k
0
votes
0
replies
1.8k
views
Answer:
A: Viral reference genomes / HCMV
9.7 years ago by
trausch
★ 2.0k
182 results • Page
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