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0
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Comment: C: Automating pre-alignment (and post-alignment) quality control
9.8 years ago by Chris Miller 22k
1
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1
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5.2k
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Comment: C: Automating pre-alignment (and post-alignment) quality control
9.8 years ago by Chris Miller 22k
2
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0
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5.4k
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Comment: C: Would a hybrid hard drive (SHDD) improve performance for high IO bioinformatics
9.8 years ago by Chris Miller 22k
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2.0k
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Comment: C: Aligning high depth data to short target sequence
9.8 years ago by Chris Miller 22k
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2.7k
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Comment: Comment: Bioinformatics for Cancer Genomics Workshop
updated 3.3 years ago by 45k • written 9.8 years ago by 22k
1
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1
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4.5k
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Comment: C: Mixed opinions on somatic variant calling method
9.8 years ago by Chris Miller 22k
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1
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6.0k
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Comment: C: HiSeq vs GA for RNASeqV2 on TCGA
9.8 years ago by Chris Miller 22k
2
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0
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3.5k
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Comment: C: Is it correct to merge TCGA mutation data from multiple centers
9.8 years ago by Chris Miller 22k
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0
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4.9k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.8 years ago by Chris Miller 22k
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1
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4.9k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.8 years ago by Chris Miller 22k
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1
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6.4k
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Answer: A: Fusion gene detection software
9.9 years ago by Chris Miller 22k
2
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0
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3.3k
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Comment: C: Did dbSNP not get the memo about hg38 chromosome names?
9.9 years ago by Chris Miller 22k
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18k
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Comment: C: TCGA/Broad Institute CNV Files Segment Mean
9.9 years ago by Chris Miller 22k
1
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0
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11k
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Answer: A: What are the terms for reference allele and alternate alleles in cancer?
10.0 years ago by Chris Miller 22k
1
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1
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3.0k
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Answer: A: genome music bmr calc-covg [Run in parallel]
10.0 years ago by Chris Miller 22k
3
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5
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5.5k
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Annotating gene fusion predictions
gene structural-variant sv annotation fusion
updated 3.2 years ago by 45k • written 10.0 years ago by 22k
0
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1
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5.5k
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Comment: C: Annotating gene fusion predictions
10.0 years ago by Chris Miller 22k
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0
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2.2k
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Comment: C: sciClone annotation help
10.1 years ago by Chris Miller 22k
3
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0
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3.0k
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Comment: C: Can I run VEP on a VCF twice?
10.1 years ago by Chris Miller 22k
1
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3
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9.3k
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Answer: Answer: Identifying FLT3-ITD with Pindel
updated 3.2 years ago by 45k • written 10.1 years ago by 22k
1
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2
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2.4k
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Answer: Answer: JISTIC. Make Probe location file to compare copy number among samples
updated 3.1 years ago by 45k • written 10.2 years ago by 22k
1
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1
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3.0k
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Answer: Answer: Effect of Read Length?
updated 3.1 years ago by 45k • written 10.2 years ago by 22k
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0
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4.6k
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Comment: C: Will Picard MarkDuplicates also un-mark duplicates?
10.2 years ago by Chris Miller 22k
1
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1
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3.7k
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Answer: Answer: What is a good threshold for calling variants in WES data
updated 2.9 years ago by 45k • written 10.3 years ago by 22k
1
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1
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1.9k
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Answer: A: About Sciclone cluster's color
10.4 years ago by Chris Miller 22k
1
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1
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3.6k
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Comment: Comment: Efficiently storing methylation data from BS-sequencing
updated 2.9 years ago by 45k • written 10.4 years ago by 22k
3
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7
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3.6k
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Efficiently storing methylation data from BS-sequencing
bsseq bisulfilte-sequencing methylation
updated 2.9 years ago by 45k • written 10.4 years ago by 22k
0
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0
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18k
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Comment: Comment: TCGA/Broad Institute CNV Files Segment Mean
updated 2.9 years ago by 45k • written 10.4 years ago by 22k
6
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0
replies
6.5k
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Answer: Answer: Tumor evolution tool for reconstructing a phylogenetic tree
updated 2.9 years ago by 45k • written 10.4 years ago by 22k
0
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0
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3.3k
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Comment: Comment: Suggested Undergraduate Courses to become a Bioinformatician
updated 2.9 years ago by 45k • written 10.4 years ago by 22k
2
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1
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4.4k
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Answer: Answer: CNV data from TCGA
updated 2.8 years ago by 45k • written 10.5 years ago by 22k
4
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0
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5.5k
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Answer: A: Copy Number Variation (CNV) segregation algorithm
10.5 years ago by Chris Miller 22k
4
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0
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7.3k
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Comment: C: The new era of bioinformatics: simple and fast tools, fewer and more informative
10.5 years ago by Chris Miller 22k
0
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1
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3.6k
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Answer: Answer: Get Allele Frequency of each SNP in RNASeq
updated 2.8 years ago by 45k • written 10.5 years ago by 22k
8
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5
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5.4k
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Exon Array Analysis Tools
gene microarray
updated 2.0 years ago by 45k • written 15.6 years ago by 22k
2
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0
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9.6k
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Comment: Comment: Optimal design for bioinformatics "lab" space?
updated 3.4 years ago by 45k • written 10.6 years ago by 22k
0
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0
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3.6k
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Comment: C: Which Somatic SNP Callers to Benchmark?
10.6 years ago by Chris Miller 22k
0
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2
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3.6k
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Answer: Answer: Which Somatic SNP Callers to Benchmark?
updated 3.4 years ago by 45k • written 10.6 years ago by 22k
1
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0
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2.4k
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Answer: Answer: How to find most common copy number changes in cancer
updated 3.5 years ago by 45k • written 10.6 years ago by 22k
0
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0
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2.5k
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Answer: A: Human genome gap file
10.6 years ago by Chris Miller 22k
0
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0
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1.5k
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Answer: A: How do I interpret the numbers
10.7 years ago by Chris Miller 22k
3
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0
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5.0k
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Answer: Answer: Recurrent de novo mutation
updated 3.9 years ago by 45k • written 10.7 years ago by 22k
2
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1
reply
3.2k
views
Answer: Answer: Why Pash 3.0 has been chosen for Roadmap Epigenome?
updated 3.5 years ago by 45k • written 10.7 years ago by 22k
1
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1
reply
26k
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Comment: Comment: How To Generate A Bibtex File From Pmids
updated 3.5 years ago by 45k • written 10.7 years ago by 22k
6
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0
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10k
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Comment: C: Notepad and word will not read Fastq or FASTA files
10.7 years ago by Chris Miller 22k
1
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0
replies
5.4k
views
Answer: Answer: Why a single gene can have multiple locations in chromosome?
updated 3.5 years ago by 45k • written 10.7 years ago by 22k
1
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0
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2.9k
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Comment: Comment: Genomic Identification of Significant Targets in Cancer
updated 3.5 years ago by 45k • written 10.7 years ago by 22k
2
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0
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2.8k
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Answer: Answer: How to aggregate multiple copy number variation profiles or select the best one
updated 3.5 years ago by 45k • written 10.7 years ago by 22k
0
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0
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5.0k
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Comment: Comment: Somaticsniper Hangs Up
updated 3.6 years ago by 45k • written 10.7 years ago by 22k
0
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0
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6.0k
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Comment: C: .bam file of human reference genome (hg19)
10.7 years ago by Chris Miller 22k
1,036 results • Page 10 of 21
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