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7
votes
2
replies
3.2k
views
Program to prioritize silent SNVs?
silent variant-annotation SNV
updated 2.3 years ago by 43k • written 9.5 years ago by ★ 3.0k
0
votes
1
reply
2.0k
views
Comment: Comment: Conservation score for intronic variants
updated 2.2 years ago by 43k • written 9.4 years ago by ★ 3.0k
1
vote
0
replies
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
0
votes
1
reply
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
0
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0
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4.7k
views
Comment: C: Whole Blood Gene Expression Deconvolution
9.4 years ago by Christian ★ 3.0k
1
vote
1
reply
7.3k
views
Comment: C: Differential gene expession analysis in cell populations of mixed tumor and norm
9.4 years ago by Christian ★ 3.0k
0
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0
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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
reply
7.3k
views
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
14
votes
12
replies
7.3k
views
7 follow
Differential gene expession analysis in cell populations of mixed tumor and normal cells
RNA-Seq DESeq EdgeR deconvolution cell-type
updated 2.2 years ago by 43k • written 9.4 years ago by ★ 3.0k
0
votes
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
vote
1
reply
25k
views
Comment: C: Genomics is not Special. Computational Biologists are reinventing the wheel for
9.5 years ago by Christian ★ 3.0k
1
vote
1
reply
9.0k
views
Comment: C: Copy Number Variation from paired end RNA-Seq data
9.5 years ago by Christian ★ 3.0k
3
votes
0
replies
9.0k
views
Answer: Answer: Copy Number Variation from paired end RNA-Seq data
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 3.0k
0
votes
0
replies
4.5k
views
Comment: C: Filter VCFs with ExAC data
9.5 years ago by Christian ★ 3.0k
1
vote
1
reply
3.5k
views
Comment: C: Pindel too slow. How to speedup
9.5 years ago by Christian ★ 3.0k
0
votes
0
replies
15k
views
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
vote
0
replies
3.2k
views
Comment: Comment: Program to prioritize silent SNVs?
updated 2.3 years ago by 43k • written 9.5 years ago by ★ 3.0k
2
votes
0
replies
13k
views
Answer: A: CNV analysis tool on exome data for NGS
9.6 years ago by Christian ★ 3.0k
5
votes
1
reply
8.3k
views
Answer: A: Curious about gene fusion in exome seuquencing data.
9.6 years ago by Christian ★ 3.0k
0
votes
1
reply
8.0k
views
Comment: C: Identifying false positives in mutect output
9.6 years ago by Christian ★ 3.0k
0
votes
4
replies
6.3k
views
Acceptable "Percentage Of Usable Bases On Target" In Exome Sequencing Experiment
exome sequencing picard
updated 2.3 years ago by 43k • written 11.0 years ago by ★ 3.0k
2
votes
2
replies
8.0k
views
Answer: A: Identifying false positives in mutect output
9.8 years ago by Christian ★ 3.0k
0
votes
1
reply
3.9k
views
Comment: C: Variants with extreme strand bias in HiSeq2500 data
9.8 years ago by Christian ★ 3.0k
0
votes
0
replies
20k
views
Comment: C: Rrna Removal In Rna-Seq Data
9.8 years ago by Christian ★ 3.0k
3
votes
0
replies
4.1k
views
Answer: Answer: I'm applying for a non-PhD bioinformatics position in your lab. What do you look
updated 2.5 years ago by 43k • written 9.8 years ago by ★ 3.0k
0
votes
0
replies
7.1k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
9.8 years ago by Christian ★ 3.0k
0
votes
0
replies
5.3k
views
Comment: C: How Can I Use Penncnv With Samples Genotyped With Cytoscan Hd?
9.9 years ago by Christian ★ 3.0k
11
votes
4
replies
1.7k
views
Forum: Should A User Be Able To Accept His/Her Own Answer?
meta
updated 14 months ago by 43k • written 11.8 years ago by ★ 3.0k
0
votes
0
replies
7.1k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
9.9 years ago by Christian ★ 3.0k
0
votes
0
replies
6.6k
views
Comment: C: Absolute/Hapseg on Exome (WES) Data?
9.9 years ago by Christian ★ 3.0k
0
votes
1
reply
18k
views
Comment: C: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
10.0 years ago by Christian ★ 3.0k
0
votes
0
replies
144k
views
Comment: C: Gnu Parallel - Parallelize Serial Command Line Programs Without Changing Them
10.0 years ago by Christian ★ 3.0k
0
votes
0
replies
129k
views
Comment: C: Is There A Free Alternative To Ingenuity Pathway Analysis?
10.0 years ago by Christian ★ 3.0k
1
vote
1
reply
3.9k
views
Answer: A: How to test the robustness and the performance of a novel classification algorit
10.0 years ago by Christian ★ 3.0k
0
votes
1
reply
7.1k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
10.0 years ago by Christian ★ 3.0k
0
votes
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
9
votes
1
reply
18k
views
Answer: Answer: Advice For Newcomers To The Bioinformatics Field
updated 18 months ago by 43k • written 10.0 years ago by ★ 3.0k
0
votes
0
replies
1.9k
views
Answer: A: Installing Goldenhelix Genomebrowse On A Server
10.0 years ago by Christian ★ 3.0k
0
votes
0
replies
2.4k
views
Answer: A: New feature: follow and unfollow posts via messages or email
10.0 years ago by Christian ★ 3.0k
4
votes
0
replies
7.0k
views
Answer: A: List of np-hard problems in biology/bioinformatics
10.0 years ago by Christian ★ 3.0k
0
votes
1
reply
13k
views
Comment: C: CNV analysis tool on exome data for NGS
10.1 years ago by Christian ★ 3.0k
0
votes
2
replies
4.5k
views
Comment: C: Multi-Sample Somatic Mutation Calling
10.1 years ago by Christian ★ 3.0k
1
vote
0
replies
9.5k
views
Answer: A: What Tool To Use To Build An Interactive Heatmap?
10.2 years ago by Christian ★ 3.0k
0
votes
1
reply
9.5k
views
Comment: C: How To Use Maf Files In The Absolute Software
10.2 years ago by Christian ★ 3.0k
0
votes
0
replies
2.8k
views
Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
10.2 years ago by Christian ★ 3.0k
0
votes
0
replies
4.7k
views
Comment: C: How To Check For Ploidy Using Ngs Only?
10.2 years ago by Christian ★ 3.0k
0
votes
1
reply
2.8k
views
Answer: A: Samtools Pileup Of Millions Of Reads From A Single Amplicon
10.2 years ago by Christian ★ 3.0k
1
vote
1
reply
2.8k
views
Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
10.2 years ago by Christian ★ 3.0k
0
votes
1
reply
4.7k
views
Comment: C: How To Check For Ploidy Using Ngs Only?
10.2 years ago by Christian ★ 3.0k
0
votes
2
replies
11k
views
Comment: C: Compute Binned Gc-Normalized Read Counts From Bam File
10.2 years ago by Christian ★ 3.0k
224 results • Page 3 of 5
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