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Answer: Answer: Protein prediction tool
10 months ago by Collin ▴ 1000
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934
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
11 months ago by Collin ▴ 1000
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934
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
11 months ago by Collin ▴ 1000
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934
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
11 months ago by Collin ▴ 1000
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1.3k
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Answer: Answer: Identification of transcription factors from a list of DEGs
11 months ago by Collin ▴ 1000
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381
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Answer: Answer: Association analysis with SNP
12 months ago by Collin ▴ 1000
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710
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Comment: Comment: Preparing CHASMplus database for annotation
12 months ago by Collin ▴ 1000
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1
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710
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Comment: Comment: Preparing CHASMplus database for annotation
13 months ago by Collin ▴ 1000
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710
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Answer: Answer: Preparing CHASMplus database for annotation
13 months ago by Collin ▴ 1000
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1.6k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
14 months ago by Collin ▴ 1000
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1.6k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
14 months ago by Collin ▴ 1000
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1.5k
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Answer: A: Is there a tool to predict if a missense variant causes a loss of function on th
updated 17 months ago by 118k • written 19 months ago by ▴ 1000
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1.5k
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Comment: C: VEP is very slow. Fork doesnt seem to work
17 months ago by Collin ▴ 1000
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1.5k
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Comment: C: VEP is very slow. Fork doesnt seem to work
17 months ago by Collin ▴ 1000
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1.5k
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Comment: C: Is there a tool to predict if a missense variant causes a loss of function on th
19 months ago by Collin ▴ 1000
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22k
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Answer: Answer: SNP annotation tool
updated 6 months ago by 36k • written 21 months ago by ▴ 1000
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1.2k
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Comment: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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830
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Comment: C: Protein_Change in MAF
21 months ago by Collin ▴ 1000
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1.2k
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Comment: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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1.2k
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Comment: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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1
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1.2k
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Comment: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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1.2k
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Comment: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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1.2k
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Answer: C: TCGA driver mutation data
21 months ago by Collin ▴ 1000
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730
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
23 months ago by Collin ▴ 1000
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730
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
23 months ago by Collin ▴ 1000
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1.9k
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Comment: C: Get clinVar info for SNP with VEP
2.2 years ago by Collin ▴ 1000
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2
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1.9k
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Comment: C: Get clinVar info for SNP with VEP
2.2 years ago by Collin ▴ 1000
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2
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1.9k
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Answer: C: Get clinVar info for SNP with VEP
2.2 years ago by Collin ▴ 1000
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1
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683
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Comment: C: Variant effect prediction
2.3 years ago by Collin ▴ 1000
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862
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Comment: C: How to go from VCF file to protein level
2.3 years ago by Collin ▴ 1000
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622
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Comment: C: Mutation clustering in protein domains
2.4 years ago by Collin ▴ 1000
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697
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Comment: C: How to download passenger mutations for cancer
2.4 years ago by Collin ▴ 1000
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697
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Comment: C: How to download passenger mutations for cancer
2.4 years ago by Collin ▴ 1000
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1
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697
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Answer: A: How to download passenger mutations for cancer
2.4 years ago by Collin ▴ 1000
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3
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5.2k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
sequencing variant annotation Cancer
updated 5 months ago by 36k • written 6.8 years ago by ▴ 1000
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519
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Answer: A: Getting a list of tumor suppressors
2.5 years ago by Collin ▴ 1000
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1
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3.2k
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Comment: C: Can't open file 'features': [Errno 2] No such file or directory
2.5 years ago by Collin ▴ 1000
2
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1
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3.2k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
2.5 years ago by Collin ▴ 1000
2
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1
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744
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Answer: A: Cancer driver mutations Identification from VCFs
2.5 years ago by Collin ▴ 1000
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809
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
2.5 years ago by Collin ▴ 1000
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1
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809
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
2.5 years ago by Collin ▴ 1000
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2.1k
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Comment: C: Interesting things to do with 23andme data
2.5 years ago by Collin ▴ 1000
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395
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Answer: A: about snp prediction
2.5 years ago by Collin ▴ 1000
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779
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Answer: A: Somatic Variant Annotation and Interpretation
2.5 years ago by Collin ▴ 1000
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3.9k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
2.7 years ago by Collin ▴ 1000
1
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1
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4.1k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 2.7 years ago by 36k • written 6.7 years ago by ▴ 1000
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1
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1.9k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 2.7 years ago by 36k • written 6.7 years ago by ▴ 1000
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3.1k
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Comment: C: pathogenicity predictors of cancer mutations
3.1 years ago by Collin ▴ 1000
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2.4k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
3.1 years ago by Collin ▴ 1000
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2.4k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
3.1 years ago by Collin ▴ 1000
120 results • Page 1 of 3
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