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Answer: A: Sequence uniformity cov
7.3 years ago by trausch ★ 1.9k
3
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5.8k
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Answer: A: Program to calculate and add the NM tag to a bam file
7.3 years ago by trausch ★ 1.9k
4
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8.2k
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Answer: A: Need help : cut the fasta sequences from a specific region
7.4 years ago by trausch ★ 1.9k
2
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3.6k
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Answer: A: How can I check the direction of DNA replication?
7.4 years ago by trausch ★ 1.9k
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5.7k
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Comment: C: QC for Whole Exome Sequence Data
7.4 years ago by trausch ★ 1.9k
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3.0k
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Answer: A: Structural Variation Discovery: Delly's Output
7.4 years ago by trausch ★ 1.9k
4
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2
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2.9k
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Answer: A: chromosomal locations of telomeric regions from the Genome
7.4 years ago by trausch ★ 1.9k
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1
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2.2k
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Comment: C: primer design tool suggestions
7.5 years ago by trausch ★ 1.9k
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3.1k
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Answer: A: Help: Phred quality for ab1 files
7.7 years ago by trausch ★ 1.9k
1
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0
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2.1k
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Answer: A: Full intronic deletions on a Whole-Exome Sequencing experiment
7.8 years ago by trausch ★ 1.9k
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0
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5.1k
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Answer: A: How/where to download Human recombination map/hotspots?
8.2 years ago by trausch ★ 1.9k
2
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1
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5.0k
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Answer: A: Filter VCF by sample?
8.2 years ago by trausch ★ 1.9k
0
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1
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2.7k
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Comment: C: Warning from lumpyexpress when calling copy number variants
8.3 years ago by trausch ★ 1.9k
0
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0
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2.9k
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Comment: C: Estimate stdev and mean in paired-end
8.3 years ago by trausch ★ 1.9k
0
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0
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7.0k
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Comment: C: Running Delly for structural Variants
8.3 years ago by trausch ★ 1.9k
0
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1
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7.0k
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Comment: C: Running Delly for structural Variants
8.3 years ago by trausch ★ 1.9k
2
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2
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7.0k
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Answer: A: Running Delly for structural Variants
8.3 years ago by trausch ★ 1.9k
0
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0
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2.9k
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Comment: C: Prioritize structural variation (SV) callings supported by multiple softwares
8.6 years ago by trausch ★ 1.9k
2
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1
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2.9k
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Comment: C: Prioritize structural variation (SV) callings supported by multiple softwares
8.6 years ago by trausch ★ 1.9k
2
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1
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4.5k
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Answer: A: Cosmic mutation signature
8.8 years ago by trausch ★ 1.9k
1
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0
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8.3k
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Comment: C: Fastq dump error
8.8 years ago by trausch ★ 1.9k
2
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1
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2.6k
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Comment: C: check whether two bam files are sequenced from the same sample
8.8 years ago by trausch ★ 1.9k
1
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0
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4.5k
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Answer: A: How to change snp ID to Variation ID of Clinvar Database
8.8 years ago by trausch ★ 1.9k
1
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0
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1.7k
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Comment: C: Are there any available genome data files in .AVRO format
8.8 years ago by trausch ★ 1.9k
3
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1
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5.5k
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Answer: C: shapeIt - prephasing - 1000g genetic map
8.8 years ago by trausch ★ 1.9k
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2.8k
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Comment: C: What could be the reason for having mutations in too many cancer samples?
8.8 years ago by trausch ★ 1.9k
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0
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1.4k
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Comment: C: Can reseq data set with different read lengths generated from Trimmomatic be use
8.8 years ago by trausch ★ 1.9k
3
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1
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8.1k
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Answer: A: What is the best way to make a bam file smaller by removing unwanted information
8.9 years ago by trausch ★ 1.9k
2
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1
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2.3k
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Answer: A: GRCh37 database, population filter
8.9 years ago by trausch ★ 1.9k
0
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2.5k
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Answer: A: checking many somatic mutations in IGV
8.9 years ago by trausch ★ 1.9k
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0
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1.6k
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Answer: A: Viral reference genomes / HCMV
8.9 years ago by trausch ★ 1.9k
181 results • Page 4 of 4
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