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Comment: Comment: How to compute physical per-base coverage from WGS paired-end reads?
updated 2.0 years ago by 43k • written 9.2 years ago by ★ 3.0k
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1
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7.6k
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Comment: C: How to compute empirical physical per-base coverage from WGS paired-end reads?
9.2 years ago by Christian ★ 3.0k
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7.2k
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Comment: Comment: Counting The Whole Insert Size From Paired-End Reads As Coverage
updated 2.0 years ago by 43k • written 9.2 years ago by ★ 3.0k
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2.1k
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Comment: C: lnkRNA gene names not recognized by DAVID
9.2 years ago by Christian ★ 3.0k
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0
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2.5k
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Comment: C: Genome Browse (Golden Helix) on a server/cluster X11 forwarded to Windows/Mac ma
9.2 years ago by Christian ★ 3.0k
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2.2k
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Comment: C: Cancer related Pathway Annotations
9.2 years ago by Christian ★ 3.0k
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2.3k
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Comment: C: Differential copy number analysis
9.4 years ago by Christian ★ 3.0k
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6.3k
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Comment: C: RNA-seq: Adjust library size using total uniquely mappable tags or only reads th
9.4 years ago by Christian ★ 3.0k
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0
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3.4k
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Comment: C: exome cnv analysis of cases only
9.4 years ago by Christian ★ 3.0k
1
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1
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3.0k
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Comment: C: Studying Bioinformatics - Reasons, motives and career
9.4 years ago by Christian ★ 3.0k
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1
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2.0k
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Comment: Comment: Conservation score for intronic variants
updated 2.2 years ago by 43k • written 9.4 years ago by ★ 3.0k
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0
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2.4k
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Comment: Comment: Any tools to predict non-coding driver mutations
updated 2.2 years ago by 43k • written 9.4 years ago by ★ 3.0k
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1
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15k
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Comment: C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
9.4 years ago by Christian ★ 3.0k
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0
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4.7k
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Comment: C: Whole Blood Gene Expression Deconvolution
9.4 years ago by Christian ★ 3.0k
1
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1
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7.3k
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Comment: C: Differential gene expession analysis in cell populations of mixed tumor and norm
9.4 years ago by Christian ★ 3.0k
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5.7k
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Comment: C: Optimum on-target coverage for exome-sequencing
9.4 years ago by Christian ★ 3.0k
0
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1
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7.3k
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Comment: Comment: Differential gene expession analysis in cell populations of mixed tumor and norm
updated 2.2 years ago by 43k • written 9.4 years ago by ★ 3.0k
0
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0
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7.3k
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Comment: C: Differential gene expession analysis in cell populations of mixed tumor and norm
9.4 years ago by Christian ★ 3.0k
1
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1
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25k
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Comment: C: Genomics is not Special. Computational Biologists are reinventing the wheel for
9.5 years ago by Christian ★ 3.0k
1
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1
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9.0k
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Comment: C: Copy Number Variation from paired end RNA-Seq data
9.5 years ago by Christian ★ 3.0k
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0
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4.5k
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Comment: C: Filter VCFs with ExAC data
9.5 years ago by Christian ★ 3.0k
1
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1
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3.5k
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Comment: C: Pindel too slow. How to speedup
9.5 years ago by Christian ★ 3.0k
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0
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15k
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Comment: C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
9.5 years ago by Christian ★ 3.0k
1
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0
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3.2k
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Comment: Comment: Program to prioritize silent SNVs?
updated 2.3 years ago by 43k • written 9.5 years ago by ★ 3.0k
0
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1
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8.0k
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Comment: C: Identifying false positives in mutect output
9.6 years ago by Christian ★ 3.0k
0
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1
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3.9k
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Comment: C: Variants with extreme strand bias in HiSeq2500 data
9.8 years ago by Christian ★ 3.0k
0
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0
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20k
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Comment: C: Rrna Removal In Rna-Seq Data
9.8 years ago by Christian ★ 3.0k
0
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0
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7.1k
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Comment: C: Is the DAVID knowledgebase not updated any more?
9.8 years ago by Christian ★ 3.0k
0
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0
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5.3k
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Comment: C: How Can I Use Penncnv With Samples Genotyped With Cytoscan Hd?
9.9 years ago by Christian ★ 3.0k
0
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0
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7.1k
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Comment: C: Is the DAVID knowledgebase not updated any more?
9.9 years ago by Christian ★ 3.0k
0
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0
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6.6k
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Comment: C: Absolute/Hapseg on Exome (WES) Data?
9.9 years ago by Christian ★ 3.0k
0
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1
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18k
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Comment: C: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
10.0 years ago by Christian ★ 3.0k
0
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0
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144k
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Comment: C: Gnu Parallel - Parallelize Serial Command Line Programs Without Changing Them
10.0 years ago by Christian ★ 3.0k
0
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0
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129k
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Comment: C: Is There A Free Alternative To Ingenuity Pathway Analysis?
10.0 years ago by Christian ★ 3.0k
0
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1
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7.1k
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Comment: C: Is the DAVID knowledgebase not updated any more?
10.0 years ago by Christian ★ 3.0k
0
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1
reply
2.4k
views
Comment: C: New feature: follow and unfollow posts via messages or email
10.0 years ago by Christian ★ 3.0k
0
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1
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13k
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Comment: C: CNV analysis tool on exome data for NGS
10.1 years ago by Christian ★ 3.0k
0
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2
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4.5k
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Comment: C: Multi-Sample Somatic Mutation Calling
10.1 years ago by Christian ★ 3.0k
0
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1
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9.5k
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Comment: C: How To Use Maf Files In The Absolute Software
10.2 years ago by Christian ★ 3.0k
0
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0
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2.8k
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Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
10.2 years ago by Christian ★ 3.0k
0
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0
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4.7k
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Comment: C: How To Check For Ploidy Using Ngs Only?
10.2 years ago by Christian ★ 3.0k
1
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1
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2.8k
views
Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
10.2 years ago by Christian ★ 3.0k
0
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1
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4.7k
views
Comment: C: How To Check For Ploidy Using Ngs Only?
10.2 years ago by Christian ★ 3.0k
0
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2
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11k
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Comment: C: Compute Binned Gc-Normalized Read Counts From Bam File
10.2 years ago by Christian ★ 3.0k
0
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2
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18k
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Comment: C: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
10.2 years ago by Christian ★ 3.0k
0
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2
replies
5.3k
views
Comment: C: How Can I Use Penncnv With Samples Genotyped With Cytoscan Hd?
10.3 years ago by Christian ★ 3.0k
0
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0
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3.3k
views
Comment: C: Absolute Accessibility On Broad
10.3 years ago by Christian ★ 3.0k
0
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1
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6.7k
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Comment: C: Makefile-Driven Workflows And Bioconductor Objects
10.3 years ago by Christian ★ 3.0k
0
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0
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2.0k
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Comment: C: How To Normalize Sequencing Coverage For Aneuploid Samples?
10.4 years ago by Christian ★ 3.0k
0
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2
replies
10k
views
Comment: C: Snakemake--Python-Based Workflow Management
10.4 years ago by Christian ★ 3.0k
133 results • Page 2 of 3
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