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Answer: A: SciClone on WES data
7.5 years ago by Chris Miller 22k
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1.6k
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Answer: A: Using ReadDepth for non-human data
7.5 years ago by Chris Miller 22k
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Answer: A: The meaning of VAF and LOH in sciclone
7.5 years ago by Chris Miller 22k
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How can I make VEP recognize header lines in my VCF?
vcf vep annotation
7.6 years ago by Chris Miller 22k
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Answer: A: How can I make VEP recognize header lines in my VCF?
7.6 years ago by Chris Miller 22k
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2.9k
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Comment: C: How can I make VEP recognize header lines in my VCF?
7.6 years ago by Chris Miller 22k
3
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1
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1.8k
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Answer: A: My translated A.A seq longer than my original Nucleotide seq!! Could someone exp
7.6 years ago by Chris Miller 22k
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3.1k
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Answer: A: Generate column names on the fly R
7.6 years ago by Chris Miller 22k
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1.6k
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Answer: A: bam-readcount values are higher than Mutect results
7.6 years ago by Chris Miller 22k
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2.8k
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Comment: C: Bam-readcount output empty from certain regions (RNA seq bams)
7.6 years ago by Chris Miller 22k
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1
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2.8k
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Answer: A: Bam-readcount output empty from certain regions (RNA seq bams)
7.6 years ago by Chris Miller 22k
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2.7k
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Answer: A: bam-readcount tool: output zero coverage bases
7.6 years ago by Chris Miller 22k
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2.0k
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Answer: A: How to plot mutation hotspot according to mutation counts
7.6 years ago by Chris Miller 22k
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Comment: C: What is Copy Number Variation(CNV) and Alteration(CNA)
7.7 years ago by Chris Miller 22k
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18k
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Comment: C: What is Copy Number Variation(CNV) and Alteration(CNA)
7.7 years ago by Chris Miller 22k
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Answer: A: What is Copy Number Variation(CNV) and Alteration(CNA)
7.7 years ago by Chris Miller 22k
4
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1
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3.4k
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Answer: A: Deciding on a Variant Caller
7.7 years ago by Chris Miller 22k
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2.1k
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Comment: C: bam-readcount error bam_header_read
7.7 years ago by Chris Miller 22k
3
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1
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4.6k
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Answer: A: SomaticSniper VS Varscan2
7.8 years ago by Chris Miller 22k
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3.6k
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Comment: C: Whole Genome Sequences somatic MAF files at TCGA
7.8 years ago by Chris Miller 22k
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2.1k
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Answer: A: Bam-readcounts min-base-quality not giving expected output
7.8 years ago by Chris Miller 22k
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0
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2.2k
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Answer: A: Regions to Exclude and useSexChromosome questions
7.8 years ago by Chris Miller 22k
4
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2
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4.6k
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Answer: A: Correcting for tumor purity in tumor evolution analysis
7.9 years ago by Chris Miller 22k
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11k
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Comment: C: fastq.gz Error: Not in gzip format
7.9 years ago by Chris Miller 22k
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1
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11k
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Comment: C: fastq.gz Error: Not in gzip format
7.9 years ago by Chris Miller 22k
4
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1
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11k
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Answer: A: fastq.gz Error: Not in gzip format
7.9 years ago by Chris Miller 22k
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1
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9.6k
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Answer: A: BAM to FASTQ
7.9 years ago by Chris Miller 22k
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3.7k
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Comment: C: How to do INDEL alignment
7.9 years ago by Chris Miller 22k
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0
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3.8k
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Comment: C: BAM to Fastq using picard and others from a desired regions
7.9 years ago by Chris Miller 22k
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2
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3.8k
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Comment: C: BAM to Fastq using picard and others from a desired regions
7.9 years ago by Chris Miller 22k
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1
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2.2k
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Comment: C: How to cite the "BED 12" format ?
8.0 years ago by Chris Miller 22k
2
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1
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3.8k
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Answer: A: BAM to Fastq using picard and others from a desired regions
8.0 years ago by Chris Miller 22k
1
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1
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3.3k
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Comment: C: What is the coverage when allele frequency is < 1?
8.0 years ago by Chris Miller 22k
1
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1
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3.3k
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Comment: C: What is the coverage when allele frequency is < 1?
8.0 years ago by Chris Miller 22k
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4.2k
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Comment: C: samtools sort generates over millions of files
8.0 years ago by Chris Miller 22k
1
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0
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3.3k
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Comment: C: What is the coverage when allele frequency is < 1?
8.0 years ago by Chris Miller 22k
2
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2
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3.3k
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Answer: A: What is the coverage when allele frequency is < 1?
8.0 years ago by Chris Miller 22k
4
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3
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4.2k
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Simulate Paired-End Bisulfite Read Data
simulation paired sequencing short
updated 8.0 years ago by • 0 • written 13.7 years ago by 22k
4
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1
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1.8k
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Answer: A: Are there any online/offline internships in bioinformatics? Stipend does not mat
8.0 years ago by Chris Miller 22k
1
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1
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5.7k
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Comment: C: How to convert bam-readcount output to BED-VAF format
8.0 years ago by Chris Miller 22k
1
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2
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5.7k
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Answer: A: How to convert bam-readcount output to BED-VAF format
8.0 years ago by Chris Miller 22k
0
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0
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4.6k
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Comment: C: sciClone input vaf file?
8.0 years ago by Chris Miller 22k
1
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1
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4.6k
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Comment: C: sciClone input vaf file?
8.0 years ago by Chris Miller 22k
1
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2
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4.6k
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Answer: A: sciClone input vaf file?
8.0 years ago by Chris Miller 22k
0
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0
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1.8k
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Comment: C: Genome Music for Enhancers and binding sites
8.0 years ago by Chris Miller 22k
286
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64
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22k
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44 follow
Forum: Bioinformatics "Cheat Sheet"
cheat sheet
updated 2.2 years ago by 88k • written 13.7 years ago by 22k
0
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3.7k
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Comment: C: sciClone:input data wrong
8.1 years ago by Chris Miller 22k
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1
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3.7k
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Comment: C: sciClone:input data wrong
8.1 years ago by Chris Miller 22k
1
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0
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3.3k
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Comment: C: Only one cluster in multiple tumor phylogeny samples
8.1 years ago by Chris Miller 22k
1
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1
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3.7k
views
Answer: A: sciClone:input data wrong
8.1 years ago by Chris Miller 22k
1,036 results • Page 6 of 21
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