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7
votes
2
replies
3.6k
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Program to prioritize silent SNVs?
silent variant-annotation SNV
updated 3.6 years ago by 45k • written 10.9 years ago by ★ 3.1k
0
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1
reply
2.2k
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Comment: Comment: Conservation score for intronic variants
updated 3.6 years ago by 45k • written 10.8 years ago by ★ 3.1k
1
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0
replies
2.8k
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Comment: Comment: Any tools to predict non-coding driver mutations
updated 3.6 years ago by 45k • written 10.8 years ago by ★ 3.1k
0
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1
reply
17k
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Comment: C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
10.8 years ago by Christian ★ 3.1k
0
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0
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5.0k
views
Comment: C: Whole Blood Gene Expression Deconvolution
10.8 years ago by Christian ★ 3.1k
1
vote
1
reply
8.4k
views
Comment: C: Differential gene expession analysis in cell populations of mixed tumor and norm
10.8 years ago by Christian ★ 3.1k
0
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0
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6.6k
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Comment: C: Optimum on-target coverage for exome-sequencing
10.8 years ago by Christian ★ 3.1k
0
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1
reply
8.4k
views
Comment: Comment: Differential gene expession analysis in cell populations of mixed tumor and norm
updated 3.6 years ago by 45k • written 10.8 years ago by ★ 3.1k
14
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12
replies
8.4k
views
7 follow
Differential gene expession analysis in cell populations of mixed tumor and normal cells
RNA-Seq DESeq EdgeR deconvolution cell-type
updated 3.6 years ago by 45k • written 10.8 years ago by ★ 3.1k
0
votes
0
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8.4k
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Comment: C: Differential gene expession analysis in cell populations of mixed tumor and norm
10.8 years ago by Christian ★ 3.1k
1
vote
1
reply
28k
views
Comment: C: Genomics is not Special. Computational Biologists are reinventing the wheel for
10.8 years ago by Christian ★ 3.1k
1
vote
1
reply
10.0k
views
Comment: C: Copy Number Variation from paired end RNA-Seq data
10.8 years ago by Christian ★ 3.1k
3
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0
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10.0k
views
Answer: Answer: Copy Number Variation from paired end RNA-Seq data
updated 3.6 years ago by 45k • written 10.8 years ago by ★ 3.1k
0
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0
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5.3k
views
Comment: C: Filter VCFs with ExAC data
10.9 years ago by Christian ★ 3.1k
1
vote
1
reply
4.1k
views
Comment: C: Pindel too slow. How to speedup
10.9 years ago by Christian ★ 3.1k
0
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0
replies
17k
views
Comment: C: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
10.9 years ago by Christian ★ 3.1k
1
vote
0
replies
3.6k
views
Comment: Comment: Program to prioritize silent SNVs?
updated 3.6 years ago by 45k • written 10.9 years ago by ★ 3.1k
2
votes
0
replies
15k
views
Answer: A: CNV analysis tool on exome data for NGS
11.0 years ago by Christian ★ 3.1k
5
votes
1
reply
9.5k
views
Answer: A: Curious about gene fusion in exome seuquencing data.
11.0 years ago by Christian ★ 3.1k
0
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1
reply
8.9k
views
Comment: C: Identifying false positives in mutect output
11.0 years ago by Christian ★ 3.1k
0
votes
4
replies
7.1k
views
Acceptable "Percentage Of Usable Bases On Target" In Exome Sequencing Experiment
exome sequencing picard
updated 3.7 years ago by 45k • written 12.4 years ago by ★ 3.1k
2
votes
2
replies
8.9k
views
Answer: A: Identifying false positives in mutect output
11.1 years ago by Christian ★ 3.1k
0
votes
1
reply
4.5k
views
Comment: C: Variants with extreme strand bias in HiSeq2500 data
11.1 years ago by Christian ★ 3.1k
0
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0
replies
23k
views
Comment: C: Rrna Removal In Rna-Seq Data
11.2 years ago by Christian ★ 3.1k
3
votes
0
replies
4.7k
views
Answer: Answer: I'm applying for a non-PhD bioinformatics position in your lab. What do you look
updated 3.9 years ago by 45k • written 11.2 years ago by ★ 3.1k
0
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0
replies
8.9k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
11.2 years ago by Christian ★ 3.1k
0
votes
0
replies
6.7k
views
Comment: C: How Can I Use Penncnv With Samples Genotyped With Cytoscan Hd?
11.3 years ago by Christian ★ 3.1k
11
votes
4
replies
2.2k
views
Forum: Should A User Be Able To Accept His/Her Own Answer?
meta
updated 2.6 years ago by 45k • written 13.2 years ago by ★ 3.1k
0
votes
0
replies
8.9k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
11.3 years ago by Christian ★ 3.1k
0
votes
0
replies
7.4k
views
Comment: C: Absolute/Hapseg on Exome (WES) Data?
11.3 years ago by Christian ★ 3.1k
0
votes
1
reply
19k
views
Comment: C: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
11.3 years ago by Christian ★ 3.1k
0
votes
0
replies
155k
views
Comment: C: Gnu Parallel - Parallelize Serial Command Line Programs Without Changing Them
11.3 years ago by Christian ★ 3.1k
0
votes
0
replies
138k
views
Comment: C: Is There A Free Alternative To Ingenuity Pathway Analysis?
11.4 years ago by Christian ★ 3.1k
1
vote
1
reply
5.1k
views
Answer: A: How to test the robustness and the performance of a novel classification algorit
11.4 years ago by Christian ★ 3.1k
0
votes
1
reply
8.9k
views
Comment: C: Is the DAVID knowledgebase not updated any more?
11.4 years ago by Christian ★ 3.1k
0
votes
1
reply
2.8k
views
Comment: C: New feature: follow and unfollow posts via messages or email
11.4 years ago by Christian ★ 3.1k
9
votes
1
reply
20k
views
Answer: Answer: Advice For Newcomers To The Bioinformatics Field
updated 2.9 years ago by 45k • written 11.4 years ago by ★ 3.1k
0
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0
replies
2.2k
views
Answer: A: Installing Goldenhelix Genomebrowse On A Server
11.4 years ago by Christian ★ 3.1k
0
votes
0
replies
2.8k
views
Answer: A: New feature: follow and unfollow posts via messages or email
11.4 years ago by Christian ★ 3.1k
4
votes
0
replies
8.1k
views
Answer: A: List of np-hard problems in biology/bioinformatics
11.4 years ago by Christian ★ 3.1k
0
votes
1
reply
15k
views
Comment: C: CNV analysis tool on exome data for NGS
11.4 years ago by Christian ★ 3.1k
0
votes
2
replies
5.2k
views
Comment: C: Multi-Sample Somatic Mutation Calling
11.5 years ago by Christian ★ 3.1k
1
vote
0
replies
10k
views
Answer: A: What Tool To Use To Build An Interactive Heatmap?
11.5 years ago by Christian ★ 3.1k
0
votes
1
reply
11k
views
Comment: C: How To Use Maf Files In The Absolute Software
11.6 years ago by Christian ★ 3.1k
0
votes
0
replies
3.5k
views
Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
11.6 years ago by Christian ★ 3.1k
0
votes
0
replies
5.4k
views
Comment: C: How To Check For Ploidy Using Ngs Only?
11.6 years ago by Christian ★ 3.1k
0
votes
1
reply
3.5k
views
Answer: A: Samtools Pileup Of Millions Of Reads From A Single Amplicon
11.6 years ago by Christian ★ 3.1k
1
vote
1
reply
3.5k
views
Comment: C: Samtools Pileup Of Millions Of Reads From A Single Amplicon
11.6 years ago by Christian ★ 3.1k
0
votes
1
reply
5.4k
views
Comment: C: How To Check For Ploidy Using Ngs Only?
11.6 years ago by Christian ★ 3.1k
0
votes
2
replies
12k
views
Comment: C: Compute Binned Gc-Normalized Read Counts From Bam File
11.6 years ago by Christian ★ 3.1k
224 results • Page 3 of 5
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