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2
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1
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4.0k
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Answer: A: find coverage of specific exomes from a bam file
6.9 years ago by trausch ★ 2.0k
1
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0
replies
4.5k
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Answer: A: Majority consensus from bam file
6.9 years ago by trausch ★ 2.0k
0
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1
reply
3.2k
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Comment: C: Other then picard better way to calculate insertmetrics from a bam file ?
7.0 years ago by trausch ★ 2.0k
0
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1
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3.2k
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Answer: A: Other then picard better way to calculate insertmetrics from a bam file ?
7.0 years ago by trausch ★ 2.0k
0
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0
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1.4k
views
Answer: A: DNA sequences from the origins of replication.
7.0 years ago by trausch ★ 2.0k
1
vote
0
replies
1.9k
views
Answer: A: Human CNV VCF for Trios from whole-genomes
7.0 years ago by trausch ★ 2.0k
0
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0
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2.0k
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Comment: C: Identification of break points for a balanced translocation
7.0 years ago by trausch ★ 2.0k
1
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1
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2.0k
views
Answer: A: Identification of break points for a balanced translocation
7.0 years ago by trausch ★ 2.0k
0
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0
replies
1.9k
views
Answer: A: calculate haloplex coverage
7.0 years ago by trausch ★ 2.0k
1
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0
replies
3.5k
views
Answer: A: Normalising RNA-seq samples from bam files for UCSC Genome browser visualization
7.1 years ago by trausch ★ 2.0k
3
votes
0
replies
17k
views
Answer: A: AB1 to FASTQ
7.1 years ago by trausch ★ 2.0k
7
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3
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14k
views
Answer: C: Mismatch and Indel statistics from BAM/SAM file
7.1 years ago by trausch ★ 2.0k
0
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0
replies
6.6k
views
Answer: A: Detecting Homozygous Insertion from Sanger Seq
7.1 years ago by trausch ★ 2.0k
0
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0
replies
2.7k
views
Answer: A: RNA-seq : Quantification problem after mapped with BBMap
7.1 years ago by trausch ★ 2.0k
0
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1
reply
8.7k
views
Comment: C: Explain the definition of DELLY output
7.2 years ago by trausch ★ 2.0k
6
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1
reply
6.0k
views
Answer: A: Get trace data for all four bases from ab1 file
7.2 years ago by trausch ★ 2.0k
0
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1
reply
3.0k
views
Comment: C: repli-seq analysis pipeline
7.2 years ago by trausch ★ 2.0k
0
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1
reply
3.0k
views
Comment: C: repli-seq analysis pipeline
7.2 years ago by trausch ★ 2.0k
0
votes
1
reply
3.0k
views
Comment: C: repli-seq analysis pipeline
7.2 years ago by trausch ★ 2.0k
1
vote
0
replies
5.1k
views
Answer: A: Splice junction sites and number of splitted reads from STAR aligned bam
7.3 years ago by trausch ★ 2.0k
2
votes
0
replies
18k
views
Answer: A: ATAC-seq DE analysis
7.3 years ago by trausch ★ 2.0k
0
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0
replies
4.0k
views
Comment: C: expected heterozygosity calculation
7.3 years ago by trausch ★ 2.0k
2
votes
0
replies
2.7k
views
Comment: C: Add AF from 1000 genomes vcf file to a different vcf file
7.3 years ago by trausch ★ 2.0k
3
votes
2
replies
2.7k
views
Answer: A: Add AF from 1000 genomes vcf file to a different vcf file
7.3 years ago by trausch ★ 2.0k
1
vote
0
replies
1.7k
views
Comment: C: Weird insert size distribution
7.4 years ago by trausch ★ 2.0k
1
vote
1
reply
8.3k
views
Comment: C: calculate ti/tv ratio in WGS data
7.4 years ago by trausch ★ 2.0k
1
vote
0
replies
8.3k
views
Answer: A: calculate ti/tv ratio in WGS data
7.4 years ago by trausch ★ 2.0k
2
votes
0
replies
16k
views
Answer: A: bam file to .bedgraph
7.4 years ago by trausch ★ 2.0k
0
votes
0
replies
2.9k
views
Answer: A: How to normalize the bam files for RNA-Seq samples for visualization
7.4 years ago by trausch ★ 2.0k
0
votes
0
replies
2.4k
views
Comment: C: SV detection software using split reads only?
7.5 years ago by trausch ★ 2.0k
0
votes
0
replies
3.1k
views
Comment: C: Calculating coverage on a list of individual genes in WES data?
7.6 years ago by trausch ★ 2.0k
1
vote
0
replies
3.1k
views
Answer: A: Calculating coverage on a list of individual genes in WES data?
7.6 years ago by trausch ★ 2.0k
1
vote
1
reply
5.3k
views
Answer: A: How to get counts data for allele specific expression analysis (ASE) from aligne
7.7 years ago by trausch ★ 2.0k
3
votes
0
replies
1.9k
views
Answer: A: Number of individuals in 1000genomes superpopulations?
7.7 years ago by trausch ★ 2.0k
2
votes
1
reply
3.2k
views
Answer: A: Primer design to do qPCR on repetitive elements
7.7 years ago by trausch ★ 2.0k
1
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0
replies
6.0k
views
Comment: C: Get trace data for all four bases from ab1 file
7.7 years ago by trausch ★ 2.0k
0
votes
0
replies
4.9k
views
Answer: A: Do I need to provide the Illumina's target region bed file for qualimap?
7.7 years ago by trausch ★ 2.0k
0
votes
0
replies
3.0k
views
Comment: C: comparison of exome data to the 1000Genomes WGS data
7.8 years ago by trausch ★ 2.0k
0
votes
1
reply
3.0k
views
Comment: A: comparison of exome data to the 1000Genomes WGS data
7.8 years ago by trausch ★ 2.0k
0
votes
0
replies
1.5k
views
Comment: C: Unusual AF data (I think)
7.9 years ago by trausch ★ 2.0k
1
vote
0
replies
7.5k
views
Answer: A: uniformity of coverage (pct > 0.2*mean) calculation/tool
8.0 years ago by trausch ★ 2.0k
0
votes
0
replies
9.2k
views
Comment: C: ATACseq with STAR and macs2
8.0 years ago by trausch ★ 2.0k
1
vote
0
replies
14k
views
Comment: C: Mismatch and Indel statistics from BAM/SAM file
8.0 years ago by trausch ★ 2.0k
0
votes
0
replies
5.1k
views
Answer: A: Calculating coverage for WGS, WES and RNASeq
8.0 years ago by trausch ★ 2.0k
1
vote
0
replies
5.0k
views
Answer: A: Structural Variant annotation
8.0 years ago by trausch ★ 2.0k
0
votes
1
reply
14k
views
Comment: C: Mismatch and Indel statistics from BAM/SAM file
8.1 years ago by trausch ★ 2.0k
3
votes
1
reply
2.6k
views
Answer: A: Soft and Hard Clipping issue - abnormal IGV profile
8.1 years ago by trausch ★ 2.0k
0
votes
1
reply
14k
views
Comment: C: Mismatch and Indel statistics from BAM/SAM file
8.1 years ago by trausch ★ 2.0k
0
votes
1
reply
7.0k
views
Comment: C: Merge multiple VCF files (same variants, same sample) into one VCF file
8.1 years ago by trausch ★ 2.0k
0
votes
1
reply
7.0k
views
Answer: A: Merge multiple VCF files (same variants, same sample) into one VCF file
8.1 years ago by trausch ★ 2.0k
182 results • Page 3 of 4
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