Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Profile
Posts
Awards
Show
all
questions
tools
blogs
news
tutorials
forum
answers
comments
Showing :
answers
4
votes
1
reply
7.4k
views
Answer:
A: How to get the list of common genes from a VennDiagram?
3.2 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
2.7k
views
Answer:
A: Annovar using VCF file
updated 3.2 years ago by
Ram
38k • written 7.1 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
856
views
Answer:
A: How to write HGVS nomination for noncoding intergenic variants
3.2 years ago by
manuel.belmadani
★ 1.3k
0
votes
1
reply
1.3k
views
Answer:
A: Clipping reads within BAM files?
3.4 years ago by
manuel.belmadani
★ 1.3k
3
votes
0
replies
5.4k
views
Answer:
A: Pheatmap row annotation multiple categories
3.4 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
741
views
Answer:
A: unsuccessful RnBeads installation
3.6 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
996
views
Answer:
A: SAM file generation problem
3.6 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
624
views
Answer:
A: Genomic screen: Benjamini-Hochberg procedure
3.6 years ago by
manuel.belmadani
★ 1.3k
2
votes
1
reply
800
views
Answer:
A: Find motif in reads and delete everything before / extract everything after
3.6 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
610
views
Answer:
A: What is best tool for Cohort data of DNA?
3.6 years ago by
manuel.belmadani
★ 1.3k
0
votes
1
reply
1.1k
views
Answer:
A: Need suggestions in subsetting the Annovar annotated VCF file
3.6 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
804
views
Answer:
A: Motif Analysis searching for NFKB/CEBPB
3.7 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
1.1k
views
Answer:
A: How to efficiently get reference bases (hg19) for a list of SNV loci (e.g., from
3.7 years ago by
manuel.belmadani
★ 1.3k
6
votes
0
replies
736
views
Answer:
A: VCF File type
3.7 years ago by
manuel.belmadani
★ 1.3k
3
votes
1
reply
6.1k
views
Answer:
A: RNA-Seq: Getting Started with Kallisto
3.7 years ago by
manuel.belmadani
★ 1.3k
0
votes
1
reply
3.0k
views
Answer:
A: InterVar and Varsome discrepancies in ACMG classification
3.7 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
1.1k
views
Answer:
C: Novel peptide identification
3.7 years ago by
manuel.belmadani
★ 1.3k
1
vote
2
replies
828
views
Answer:
A: All result in one file
updated 3.8 years ago by
zx8754
11k • written 3.8 years ago by
manuel.belmadani
★ 1.3k
2
votes
0
replies
3.3k
views
Answer:
A: How to obtain transcript level TPM using stringtie?
3.8 years ago by
manuel.belmadani
★ 1.3k
3
votes
2
replies
11k
views
Answer:
A: Question: How to run several one-way ANOVAs in R using on different categories?
3.8 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
2.6k
views
Answer:
A: y-axis on Volcano plot
3.8 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
2.0k
views
Answer:
A: intersection for several file
3.8 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
2.1k
views
Answer:
A: Empty BAM file upon mapping with STAR
3.9 years ago by
manuel.belmadani
★ 1.3k
2
votes
0
replies
3.6k
views
Answer:
A: Code golf: detecting homopolymers of length N in the (human) genome
3.9 years ago by
manuel.belmadani
★ 1.3k
2
votes
1
reply
1.2k
views
Answer:
A: What is the statistics test on proportion data
3.9 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
3.8k
views
Answer:
A: gnomAD: query utilitites
3.9 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
2.9k
views
Answer:
A: RPM data analysis with DESeq2
3.9 years ago by
manuel.belmadani
★ 1.3k
1
vote
2
replies
1.8k
views
Answer:
A: HGVS format to VCF from portal.gdc.cancer.gov
3.9 years ago by
manuel.belmadani
★ 1.3k
3
votes
1
reply
1.7k
views
Answer:
A: In R or Python, How do I implement an allele sequence "autocomplete" tool given
4.0 years ago by
manuel.belmadani
★ 1.3k
0
votes
1
reply
1.6k
views
Answer:
A: random sampling genome.fa
4.0 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
873
views
Answer:
A: Looking for tool recommendations for text mining
4.0 years ago by
manuel.belmadani
★ 1.3k
5
votes
1
reply
4.7k
views
Answer:
A: How to combine multiple data files by column names?
4.0 years ago by
manuel.belmadani
★ 1.3k
3
votes
1
reply
1.9k
views
Answer:
A: Simple FASTQ/A manipulation... how to add a single adapter sequence to 3' of all
4.0 years ago by
manuel.belmadani
★ 1.3k
2
votes
0
replies
1.3k
views
Answer:
A: How to create a tab delimited file?
4.0 years ago by
manuel.belmadani
★ 1.3k
1
vote
2
replies
3.1k
views
Answer:
C: Why my Hisat2 result is 0% aligned concordantly and HTseq result is 100% not ali
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
2.3k
views
Answer:
A: Where to Download Cancer Raw Reads (fastq)?
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
1.1k
views
Answer:
A: Understanding Bowtie output
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
6.0k
views
Answer:
A: Creation of a VCF file from scratch with python
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
1.7k
views
Answer:
A: Cannot identify software used to make image
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
3.7k
views
Answer:
A: Principal component analysis: PC2 contribute more to variance than PC1?
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
1.3k
views
Answer:
C: BSc Thesis "Machine learning application in diagnosis of a genetic diseases" - I
4.1 years ago by
manuel.belmadani
★ 1.3k
0
votes
1
reply
4.9k
views
Answer:
A: How to extract total allele frequency from gnomAD annotation
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
2
replies
990
views
Answer:
A: how to go from aligning forward when analyzing whole exome sequencing
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
0
replies
2.0k
views
Answer:
A: Remove low quality base calls from reads
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
1.1k
views
Answer:
A: Seeking for a Linux based script ?
4.1 years ago by
manuel.belmadani
★ 1.3k
7
votes
3
replies
9.5k
views
Answer:
A: Reproducing this plot in R
4.1 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
6.2k
views
Answer:
A: PolyPhen Humdiv vs HumVar discrepancies
4.1 years ago by
manuel.belmadani
★ 1.3k
0
votes
0
replies
2.0k
views
Answer:
A: same transcript id with STAR quant mode
4.1 years ago by
manuel.belmadani
★ 1.3k
3
votes
3
replies
8.9k
views
Answer:
A: STAR or Bowtie for small RNA seq?
4.1 years ago by
manuel.belmadani
★ 1.3k
1
vote
1
reply
1.7k
views
Answer:
A: Noob question about reading SNP results from BAM file visually
4.2 years ago by
manuel.belmadani
★ 1.3k
66 results • Page
1 of 2
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6