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1.9k
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Answer:
A: Computer logistics of comparing genomes within same individual
6.3 years ago by
Chris Miller
22k
0
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0
replies
1.1k
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Answer:
A: Does bisulfite sequencing need higher sequencing depth than regular genomic sequ
6.3 years ago by
Chris Miller
22k
2
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1
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1.8k
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Answer:
A: ExAC includes WES of phenotyped population
6.3 years ago by
Chris Miller
22k
3
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1
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2.5k
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Answer:
A: R package information
6.3 years ago by
Chris Miller
22k
1
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1
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2.3k
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Answer:
A: N in fastq data
6.4 years ago by
Chris Miller
22k
0
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2
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2.2k
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Answer:
A: pipeline for neo-antigen identification
6.4 years ago by
Chris Miller
22k
4
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5.9k
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Answer:
A: Google announces DeepVariant
6.4 years ago by
Chris Miller
22k
13
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3
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5.9k
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Answer:
A: Google announces DeepVariant
6.4 years ago by
Chris Miller
22k
2
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1
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1.6k
views
Answer:
A: Finding a variant's flanking sequence
6.5 years ago by
Chris Miller
22k
3
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1
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2.1k
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Answer:
A: SciClone: Which Variant to Which Clone
6.5 years ago by
Chris Miller
22k
0
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2.7k
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Answer:
A: NGS on cancer tumor
6.5 years ago by
Chris Miller
22k
1
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0
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4.2k
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Answer:
A: Survey/Vote: If you could double the speed of any three commandline tools, which
6.5 years ago by
Chris Miller
22k
4
votes
2
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4.2k
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Answer:
A: Survey/Vote: If you could double the speed of any three commandline tools, which
6.5 years ago by
Chris Miller
22k
3
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1.8k
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Answer:
A: Mapping mutations to TCGA samples
6.5 years ago by
Chris Miller
22k
2
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0
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9.7k
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Answer:
A: perplexity value in t-sne algorithm
6.5 years ago by
Chris Miller
22k
3
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3
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2.8k
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Answer:
A: how to read indexed bamfiles
6.6 years ago by
Chris Miller
22k
1
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0
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1.7k
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Answer:
A: SciClone Cluster Number
6.6 years ago by
Chris Miller
22k
0
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1.4k
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Answer:
A: Does Genome MuSiC use soft-clipped bases in its coverage calculation?
6.6 years ago by
Chris Miller
22k
4
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1
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4.6k
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Answer:
A: Concept of Matched normal vs. Virtual Normal
6.6 years ago by
Chris Miller
22k
1
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1
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10k
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Answer:
A: CNV detection from RNA-seq data
6.6 years ago by
Chris Miller
22k
2
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2.4k
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Answer:
A: sciClone: usage for inferring tumor clonality
6.6 years ago by
Chris Miller
22k
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3.1k
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Answer:
A: Tumor purity estimation by allele frequency of COSMIC identified somatic mutatio
6.7 years ago by
Chris Miller
22k
0
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1
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15k
views
Answer:
A: Unable to access jarfile trimmomatic-0.35
6.7 years ago by
Chris Miller
22k
2
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0
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12k
views
Answer:
A: Unlisting lists inside data frame and collapsing their values in R
6.7 years ago by
Chris Miller
22k
0
votes
0
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1.6k
views
Answer:
A: sciClone: Multiple alleles at single position
6.8 years ago by
Chris Miller
22k
0
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1
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1.3k
views
Answer:
A: Low reads mapping in methylation sequencing
6.8 years ago by
Chris Miller
22k
2
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0
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2.1k
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Answer:
A: "TRUE" instead of "T" allele in R
6.9 years ago by
Chris Miller
22k
2
votes
0
replies
5.9k
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Answer:
A: TCGA clinical data, info about treatment_id / drug
6.9 years ago by
Chris Miller
22k
0
votes
0
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2.3k
views
Answer:
A: Error when running Genome MuSiC: no smg genes
6.9 years ago by
Chris Miller
22k
1
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1
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1.7k
views
Answer:
A: overlap BED files, but account for region name
6.9 years ago by
Chris Miller
22k
3
votes
1
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2.4k
views
Answer:
A: why are RNA-seq fkpm of TCGA PAN-cancer normal and primary tumor are the same
6.9 years ago by
Chris Miller
22k
1
vote
0
replies
5.6k
views
Answer:
A: How to quickly count the number of reads at a specific coordinate in a bam file
6.9 years ago by
Chris Miller
22k
0
votes
0
replies
3.6k
views
Answer:
A: SciClone on WES data
6.9 years ago by
Chris Miller
22k
0
votes
0
replies
1.5k
views
Answer:
A: Using ReadDepth for non-human data
6.9 years ago by
Chris Miller
22k
1
vote
1
reply
4.0k
views
Answer:
A: The meaning of VAF and LOH in sciclone
7.0 years ago by
Chris Miller
22k
2
votes
0
replies
2.7k
views
Answer:
A: How can I make VEP recognize header lines in my VCF?
7.0 years ago by
Chris Miller
22k
3
votes
1
reply
1.7k
views
Answer:
A: My translated A.A seq longer than my original Nucleotide seq!! Could someone exp
7.0 years ago by
Chris Miller
22k
0
votes
1
reply
2.9k
views
Answer:
A: Generate column names on the fly R
7.1 years ago by
Chris Miller
22k
0
votes
0
replies
1.6k
views
Answer:
A: bam-readcount values are higher than Mutect results
7.1 years ago by
Chris Miller
22k
0
votes
1
reply
2.6k
views
Answer:
A: Bam-readcount output empty from certain regions (RNA seq bams)
7.1 years ago by
Chris Miller
22k
0
votes
0
replies
2.5k
views
Answer:
A: bam-readcount tool: output zero coverage bases
7.1 years ago by
Chris Miller
22k
2
votes
1
reply
1.9k
views
Answer:
A: How to plot mutation hotspot according to mutation counts
7.1 years ago by
Chris Miller
22k
10
votes
1
reply
17k
views
Answer:
A: What is Copy Number Variation(CNV) and Alteration(CNA)
7.1 years ago by
Chris Miller
22k
4
votes
1
reply
3.2k
views
Answer:
A: Deciding on a Variant Caller
7.2 years ago by
Chris Miller
22k
3
votes
1
reply
4.4k
views
Answer:
A: SomaticSniper VS Varscan2
7.2 years ago by
Chris Miller
22k
0
votes
0
replies
2.0k
views
Answer:
A: Bam-readcounts min-base-quality not giving expected output
7.3 years ago by
Chris Miller
22k
0
votes
0
replies
2.2k
views
Answer:
A: Regions to Exclude and useSexChromosome questions
7.3 years ago by
Chris Miller
22k
4
votes
2
replies
4.3k
views
Answer:
A: Correcting for tumor purity in tumor evolution analysis
7.3 years ago by
Chris Miller
22k
4
votes
1
reply
10.0k
views
Answer:
A: fastq.gz Error: Not in gzip format
7.4 years ago by
Chris Miller
22k
3
votes
1
reply
8.7k
views
Answer:
A: BAM to FASTQ
7.4 years ago by
Chris Miller
22k
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