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963
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Comment: Comment: guppy basecaller giving error while basecalling
10 months ago by Medhat 9.7k
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614
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Comment: Comment: More Efficient: Whole Genome VCF splitting with and without tbi file
10 months ago by Medhat 9.7k
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688
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Answer: Answer: Need help editing text in the shell
10 months ago by Medhat 9.7k
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1.1k
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Comment: Comment: What are your preferred programs for processing DNA long reads? (de novo assembl
10 months ago by Medhat 9.7k
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1
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1.2k
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Comment: Comment: Why some insertions are symbolic in ALT column?
10 months ago by Medhat 9.7k
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1
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1.5k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
11 months ago by Medhat 9.7k
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1
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1.5k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
11 months ago by Medhat 9.7k
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679
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Comment: Comment: Variant calling analysis
11 months ago by Medhat 9.7k
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1
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679
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Comment: Comment: Variant calling analysis
11 months ago by Medhat 9.7k
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522
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Comment: Comment: Do we have any disease specific SNVs database?
13 months ago by Medhat 9.7k
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4.8k
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Comment: Comment: conda create env using .yml file leads to dependency conflicts
14 months ago by Medhat 9.7k
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1
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1.5k
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Comment: Comment: GATK showing error of reference file index
14 months ago by Medhat 9.7k
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511
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Comment: Comment: Methods for downsampling coverage in a VCF
14 months ago by Medhat 9.7k
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1
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900
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Comment: Comment: I have a reference genome explained by accession number instead of chromosome nu
14 months ago by Medhat 9.7k
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2
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2.4k
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Comment: Comment: SV calling using giraffe/vg
15 months ago by Medhat 9.7k
4
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731
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Comment: Comment: BIOINFORMATICS
15 months ago by Medhat 9.7k
2
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849
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Comment: Comment: Looking for tools to individuate gene-gene correlations from a few candidates
15 months ago by Medhat 9.7k
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951
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Comment: Comment: No CR tag in the sam file mapped by STARsolo (10x v3.1 data)
16 months ago by Medhat 9.7k
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1.6k
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Comment: Comment: Different results in finding human sequences from metagenomes (bowtie2 and Krake
16 months ago by Medhat 9.7k
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1.1k
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Comment: Comment: bedtools intersect multiple files using for loop
17 months ago by Medhat 9.7k
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1
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1.1k
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Comment: Comment: bedtools intersect multiple files using for loop
17 months ago by Medhat 9.7k
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0
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894
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Comment: Comment: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Cen
17 months ago by Medhat 9.7k
0
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1
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894
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Job: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS TGS
updated 10 months ago by 43k • written 22 months ago by 9.7k
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1
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1.2k
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Comment: Comment: Introducing Cramino: a *fast* QC tool for long reads
17 months ago by Medhat 9.7k
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1
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923
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Comment: Comment: For loop RNA Sequencing alignment
18 months ago by Medhat 9.7k
2
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1.2k
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Comment: Comment: sorting multiple .bam files in linux cluster
19 months ago by Medhat 9.7k
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0
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999
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Comment: Comment: gosling.js and React 1.7+
20 months ago by Medhat 9.7k
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1
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999
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Comment: Comment: gosling.js and React 1.7+
20 months ago by Medhat 9.7k
1
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1
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1.1k
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Comment: Comment: Leaky RNA
20 months ago by Medhat 9.7k
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0
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905
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Comment: Comment: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Seq
20 months ago by Medhat 9.7k
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1
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1.3k
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Comment: Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
21 months ago by Medhat 9.7k
0
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0
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815
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Comment: Comment: getting the coordinates of mapped regions from a bam file
21 months ago by Medhat 9.7k
1
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0
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1.3k
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Comment: Comment: Programming languages in industry
21 months ago by Medhat 9.7k
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0
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1.3k
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Comment: Comment: Programming languages in industry
21 months ago by Medhat 9.7k
2
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1
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1.3k
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Answer: Answer: Programming languages in industry
21 months ago by Medhat 9.7k
0
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1
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905
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Job: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS TGS
updated 10 months ago by 43k • written 22 months ago by 9.7k
4
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3
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2.9k
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Split VCF file
vcf sequencing
written 7.3 years ago by 9.7k
0
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0
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929
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Comment: Comment: Source of soft clipped reads from target sequencing
23 months ago by Medhat 9.7k
1
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0
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1.5k
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Answer: Answer: VCF Statistics
23 months ago by Medhat 9.7k
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1
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571
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Comment: Comment: Align chimpanzee genome
23 months ago by Medhat 9.7k
2
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1
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2.5k
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Answer: Answer: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
23 months ago by Medhat 9.7k
0
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0
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988
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Job: Postdoctoral Fellow Pacific Northwest Research Institute (PNRI) in Seattle
variants NGS
updated 22 months ago by 43k • written 23 months ago by 9.7k
1
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0
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739
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Comment: Comment: How to generate a bam file with reads of only a certain length?
24 months ago by Medhat 9.7k
1
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1
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739
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Comment: Comment: How to generate a bam file with reads of only a certain length?
24 months ago by Medhat 9.7k
0
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0
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705
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Comment: Comment: how to visulize structure variants
24 months ago by Medhat 9.7k
2
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1
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705
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Answer: Answer: how to visulize structure variants
24 months ago by Medhat 9.7k
1
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2
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4.7k
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Using PRINSEQ lite with zipped paired-end illumina reads
prinseq next-gen-sequencing quality-reads Illumina
updated 2.0 years ago by • 0 • written 9.6 years ago by 9.7k
0
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0
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941
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Comment: Comment: liftOver input file
2.1 years ago by Medhat 9.7k
0
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0
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1.7k
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Comment: Comment: How to extract reads that support the structural variants using the vcf file and
2.2 years ago by Medhat 9.7k
76
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14
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16k
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15 follow
Tutorial: List Of Bioinformatics Books
books
updated 14 months ago by 43k • written 10.9 years ago by 9.7k
1,007 results • Page 1 of 21
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