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
0
votes
0
replies
921
views
Comment:
Comment: guppy basecaller giving error while basecalling
9 months ago by
Medhat
9.7k
0
votes
0
replies
591
views
Comment:
Comment: More Efficient: Whole Genome VCF splitting with and without tbi file
9 months ago by
Medhat
9.7k
3
votes
1
reply
670
views
Answer:
Answer: Need help editing text in the shell
9 months ago by
Medhat
9.7k
1
vote
0
replies
1.1k
views
Comment:
Comment: What are your preferred programs for processing DNA long reads? (de novo assembl
9 months ago by
Medhat
9.7k
0
votes
1
reply
1.1k
views
Comment:
Comment: Why some insertions are symbolic in ALT column?
9 months ago by
Medhat
9.7k
0
votes
1
reply
1.4k
views
Comment:
Comment: Problem with GPU guppy_basecaller and SLURM
10 months ago by
Medhat
9.7k
0
votes
1
reply
1.4k
views
Comment:
Comment: Problem with GPU guppy_basecaller and SLURM
10 months ago by
Medhat
9.7k
0
votes
0
replies
649
views
Comment:
Comment: Variant calling analysis
10 months ago by
Medhat
9.7k
1
vote
1
reply
649
views
Comment:
Comment: Variant calling analysis
10 months ago by
Medhat
9.7k
0
votes
0
replies
510
views
Comment:
Comment: Do we have any disease specific SNVs database?
13 months ago by
Medhat
9.7k
0
votes
0
replies
4.6k
views
Comment:
Comment: conda create env using .yml file leads to dependency conflicts
13 months ago by
Medhat
9.7k
0
votes
1
reply
1.5k
views
Comment:
Comment: GATK showing error of reference file index
13 months ago by
Medhat
9.7k
0
votes
0
replies
490
views
Comment:
Comment: Methods for downsampling coverage in a VCF
13 months ago by
Medhat
9.7k
0
votes
1
reply
868
views
Comment:
Comment: I have a reference genome explained by accession number instead of chromosome nu
14 months ago by
Medhat
9.7k
1
vote
2
replies
2.3k
views
Comment:
Comment: SV calling using giraffe/vg
14 months ago by
Medhat
9.7k
4
votes
0
replies
700
views
Comment:
Comment: BIOINFORMATICS
14 months ago by
Medhat
9.7k
2
votes
0
replies
812
views
Comment:
Comment: Looking for tools to individuate gene-gene correlations from a few candidates
15 months ago by
Medhat
9.7k
0
votes
0
replies
924
views
Comment:
Comment: No CR tag in the sam file mapped by STARsolo (10x v3.1 data)
15 months ago by
Medhat
9.7k
0
votes
0
replies
1.6k
views
Comment:
Comment: Different results in finding human sequences from metagenomes (bowtie2 and Krake
15 months ago by
Medhat
9.7k
0
votes
0
replies
1.1k
views
Comment:
Comment: bedtools intersect multiple files using for loop
16 months ago by
Medhat
9.7k
1
vote
1
reply
1.1k
views
Comment:
Comment: bedtools intersect multiple files using for loop
16 months ago by
Medhat
9.7k
0
votes
0
replies
871
views
Comment:
Comment: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Cen
16 months ago by
Medhat
9.7k
0
votes
1
reply
871
views
Job:
Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS
TGS
updated 9 months ago by
Ram
43k • written 21 months ago by
Medhat
9.7k
0
votes
1
reply
1.2k
views
Comment:
Comment: Introducing Cramino: a *fast* QC tool for long reads
17 months ago by
Medhat
9.7k
0
votes
1
reply
893
views
Comment:
Comment: For loop RNA Sequencing alignment
17 months ago by
Medhat
9.7k
2
votes
0
replies
1.1k
views
Comment:
Comment: sorting multiple .bam files in linux cluster
18 months ago by
Medhat
9.7k
0
votes
0
replies
964
views
Comment:
Comment: gosling.js and React 1.7+
19 months ago by
Medhat
9.7k
0
votes
1
reply
964
views
Comment:
Comment: gosling.js and React 1.7+
19 months ago by
Medhat
9.7k
1
vote
1
reply
1.1k
views
Comment:
Comment: Leaky RNA
19 months ago by
Medhat
9.7k
0
votes
0
replies
886
views
Comment:
Comment: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Seq
20 months ago by
Medhat
9.7k
0
votes
1
reply
1.2k
views
Comment:
Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
20 months ago by
Medhat
9.7k
0
votes
0
replies
790
views
Comment:
Comment: getting the coordinates of mapped regions from a bam file
21 months ago by
Medhat
9.7k
1
vote
0
replies
1.2k
views
Comment:
Comment: Programming languages in industry
21 months ago by
Medhat
9.7k
0
votes
0
replies
1.2k
views
Comment:
Comment: Programming languages in industry
21 months ago by
Medhat
9.7k
2
votes
1
reply
1.2k
views
Answer:
Answer: Programming languages in industry
21 months ago by
Medhat
9.7k
0
votes
1
reply
886
views
Job:
Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS
TGS
updated 9 months ago by
Ram
43k • written 21 months ago by
Medhat
9.7k
4
votes
3
replies
2.9k
views
Split VCF file
vcf
sequencing
written 7.2 years ago by
Medhat
9.7k
0
votes
0
replies
890
views
Comment:
Comment: Source of soft clipped reads from target sequencing
22 months ago by
Medhat
9.7k
1
vote
0
replies
1.5k
views
Answer:
Answer: VCF Statistics
22 months ago by
Medhat
9.7k
0
votes
1
reply
539
views
Comment:
Comment: Align chimpanzee genome
22 months ago by
Medhat
9.7k
2
votes
1
reply
2.3k
views
Answer:
Answer: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
22 months ago by
Medhat
9.7k
0
votes
0
replies
961
views
Job:
Postdoctoral Fellow Pacific Northwest Research Institute (PNRI) in Seattle
variants
NGS
updated 21 months ago by
Ram
43k • written 23 months ago by
Medhat
9.7k
1
vote
0
replies
711
views
Comment:
Comment: How to generate a bam file with reads of only a certain length?
23 months ago by
Medhat
9.7k
1
vote
1
reply
711
views
Comment:
Comment: How to generate a bam file with reads of only a certain length?
23 months ago by
Medhat
9.7k
0
votes
0
replies
677
views
Comment:
Comment: how to visulize structure variants
23 months ago by
Medhat
9.7k
2
votes
1
reply
677
views
Answer:
Answer: how to visulize structure variants
23 months ago by
Medhat
9.7k
1
vote
2
replies
4.7k
views
Using PRINSEQ lite with zipped paired-end illumina reads
prinseq
next-gen-sequencing
quality-reads
Illumina
updated 23 months ago by
Simo Njabulo Maduna
• 0 • written 9.5 years ago by
Medhat
9.7k
0
votes
0
replies
918
views
Comment:
Comment: liftOver input file
2.1 years ago by
Medhat
9.7k
0
votes
0
replies
1.7k
views
Comment:
Comment: How to extract reads that support the structural variants using the vcf file and
2.2 years ago by
Medhat
9.7k
75
votes
14
replies
16k
views
15 follow
Tutorial:
List Of Bioinformatics Books
books
updated 13 months ago by
Ram
43k • written 10.9 years ago by
Medhat
9.7k
1,007 results • Page
1 of 21
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