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1
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Answer: A: Majority consensus from bam file
6.1 years ago by trausch ★ 1.9k
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1
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2.5k
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Comment: C: Other then picard better way to calculate insertmetrics from a bam file ?
6.2 years ago by trausch ★ 1.9k
0
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1
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2.5k
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Answer: A: Other then picard better way to calculate insertmetrics from a bam file ?
6.2 years ago by trausch ★ 1.9k
0
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1.1k
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Answer: A: DNA sequences from the origins of replication.
6.2 years ago by trausch ★ 1.9k
1
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1.6k
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Answer: A: Human CNV VCF for Trios from whole-genomes
6.2 years ago by trausch ★ 1.9k
0
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0
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1.7k
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Comment: C: Identification of break points for a balanced translocation
6.2 years ago by trausch ★ 1.9k
1
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1
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1.7k
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Answer: A: Identification of break points for a balanced translocation
6.2 years ago by trausch ★ 1.9k
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1.6k
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Answer: A: calculate haloplex coverage
6.2 years ago by trausch ★ 1.9k
1
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0
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3.0k
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Answer: A: Normalising RNA-seq samples from bam files for UCSC Genome browser visualization
6.3 years ago by trausch ★ 1.9k
2
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0
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14k
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Answer: A: AB1 to FASTQ
6.3 years ago by trausch ★ 1.9k
7
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3
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12k
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Answer: C: Mismatch and Indel statistics from BAM/SAM file
6.3 years ago by trausch ★ 1.9k
0
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0
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5.9k
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Answer: A: Detecting Homozygous Insertion from Sanger Seq
6.3 years ago by trausch ★ 1.9k
0
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0
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2.2k
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Answer: A: RNA-seq : Quantification problem after mapped with BBMap
6.3 years ago by trausch ★ 1.9k
0
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1
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7.6k
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Comment: C: Explain the definition of DELLY output
6.3 years ago by trausch ★ 1.9k
6
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1
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5.4k
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Answer: A: Get trace data for all four bases from ab1 file
6.4 years ago by trausch ★ 1.9k
0
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1
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2.7k
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Comment: C: repli-seq analysis pipeline
6.4 years ago by trausch ★ 1.9k
0
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1
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2.7k
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Comment: C: repli-seq analysis pipeline
6.4 years ago by trausch ★ 1.9k
0
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1
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2.7k
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Comment: C: repli-seq analysis pipeline
6.4 years ago by trausch ★ 1.9k
1
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0
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3.9k
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Answer: A: Splice junction sites and number of splitted reads from STAR aligned bam
6.4 years ago by trausch ★ 1.9k
2
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0
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15k
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Answer: A: ATAC-seq DE analysis
6.4 years ago by trausch ★ 1.9k
0
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0
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3.8k
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Comment: C: expected heterozygosity calculation
6.5 years ago by trausch ★ 1.9k
2
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0
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2.4k
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Comment: C: Add AF from 1000 genomes vcf file to a different vcf file
6.5 years ago by trausch ★ 1.9k
3
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2
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2.4k
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Answer: A: Add AF from 1000 genomes vcf file to a different vcf file
6.5 years ago by trausch ★ 1.9k
1
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0
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1.5k
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Comment: C: Weird insert size distribution
6.5 years ago by trausch ★ 1.9k
1
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1
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7.3k
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Comment: C: calculate ti/tv ratio in WGS data
6.5 years ago by trausch ★ 1.9k
1
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0
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7.3k
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Answer: A: calculate ti/tv ratio in WGS data
6.6 years ago by trausch ★ 1.9k
2
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0
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15k
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Answer: A: bam file to .bedgraph
6.6 years ago by trausch ★ 1.9k
0
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0
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2.7k
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Answer: A: How to normalize the bam files for RNA-Seq samples for visualization
6.6 years ago by trausch ★ 1.9k
0
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0
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2.0k
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Comment: C: SV detection software using split reads only?
6.7 years ago by trausch ★ 1.9k
0
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0
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2.9k
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Comment: C: Calculating coverage on a list of individual genes in WES data?
6.8 years ago by trausch ★ 1.9k
1
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0
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2.9k
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Answer: A: Calculating coverage on a list of individual genes in WES data?
6.8 years ago by trausch ★ 1.9k
1
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1
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4.5k
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Answer: A: How to get counts data for allele specific expression analysis (ASE) from aligne
6.8 years ago by trausch ★ 1.9k
3
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0
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1.7k
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Answer: A: Number of individuals in 1000genomes superpopulations?
6.8 years ago by trausch ★ 1.9k
2
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1
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2.6k
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Answer: A: Primer design to do qPCR on repetitive elements
6.9 years ago by trausch ★ 1.9k
1
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0
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5.4k
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Comment: C: Get trace data for all four bases from ab1 file
6.9 years ago by trausch ★ 1.9k
0
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0
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4.3k
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Answer: A: Do I need to provide the Illumina's target region bed file for qualimap?
6.9 years ago by trausch ★ 1.9k
0
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0
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2.6k
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Comment: C: comparison of exome data to the 1000Genomes WGS data
7.0 years ago by trausch ★ 1.9k
0
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1
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2.6k
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Comment: A: comparison of exome data to the 1000Genomes WGS data
7.0 years ago by trausch ★ 1.9k
0
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0
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1.3k
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Comment: C: Unusual AF data (I think)
7.0 years ago by trausch ★ 1.9k
1
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0
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6.6k
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Answer: A: uniformity of coverage (pct > 0.2*mean) calculation/tool
7.1 years ago by trausch ★ 1.9k
0
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0
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8.3k
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Comment: C: ATACseq with STAR and macs2
7.2 years ago by trausch ★ 1.9k
1
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0
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12k
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Comment: C: Mismatch and Indel statistics from BAM/SAM file
7.2 years ago by trausch ★ 1.9k
0
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0
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4.5k
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Answer: A: Calculating coverage for WGS, WES and RNASeq
7.2 years ago by trausch ★ 1.9k
1
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0
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4.1k
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Answer: A: Structural Variant annotation
7.2 years ago by trausch ★ 1.9k
0
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1
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12k
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Comment: C: Mismatch and Indel statistics from BAM/SAM file
7.2 years ago by trausch ★ 1.9k
3
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1
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2.4k
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Answer: A: Soft and Hard Clipping issue - abnormal IGV profile
7.2 years ago by trausch ★ 1.9k
0
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1
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12k
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Comment: C: Mismatch and Indel statistics from BAM/SAM file
7.2 years ago by trausch ★ 1.9k
0
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1
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6.4k
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Comment: C: Merge multiple VCF files (same variants, same sample) into one VCF file
7.3 years ago by trausch ★ 1.9k
0
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1
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6.4k
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Answer: A: Merge multiple VCF files (same variants, same sample) into one VCF file
7.3 years ago by trausch ★ 1.9k
0
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1
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2.8k
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Comment: C: Problems getting read number per gene after sequencing
7.3 years ago by trausch ★ 1.9k
181 results • Page 3 of 4
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