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2
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2
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637
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Answer: Answer: Set the same Y scale for different plots
18 days ago by Medhat 9.7k
0
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0
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2.9k
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Comment: Comment: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
6 weeks ago by Medhat 9.7k
0
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0
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1.0k
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Comment: Comment: guppy basecaller giving error while basecalling
12 months ago by Medhat 9.7k
0
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0
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657
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Comment: Comment: More Efficient: Whole Genome VCF splitting with and without tbi file
12 months ago by Medhat 9.7k
3
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1
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735
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Answer: Answer: Need help editing text in the shell
12 months ago by Medhat 9.7k
1
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0
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1.3k
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Comment: Comment: What are your preferred programs for processing DNA long reads? (de novo assembl
12 months ago by Medhat 9.7k
0
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1
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1.3k
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Comment: Comment: Why some insertions are symbolic in ALT column?
12 months ago by Medhat 9.7k
0
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1
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1.6k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
12 months ago by Medhat 9.7k
0
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1
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1.6k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
12 months ago by Medhat 9.7k
0
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0
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733
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Comment: Comment: Variant calling analysis
13 months ago by Medhat 9.7k
1
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1
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733
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Comment: Comment: Variant calling analysis
13 months ago by Medhat 9.7k
0
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0
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566
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Comment: Comment: Do we have any disease specific SNVs database?
15 months ago by Medhat 9.7k
0
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0
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5.5k
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Comment: Comment: conda create env using .yml file leads to dependency conflicts
15 months ago by Medhat 9.7k
0
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1
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1.7k
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Comment: Comment: GATK showing error of reference file index
16 months ago by Medhat 9.7k
0
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0
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557
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Comment: Comment: Methods for downsampling coverage in a VCF
16 months ago by Medhat 9.7k
0
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1
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959
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Comment: Comment: I have a reference genome explained by accession number instead of chromosome nu
16 months ago by Medhat 9.7k
1
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2
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2.6k
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Comment: Comment: SV calling using giraffe/vg
17 months ago by Medhat 9.7k
4
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0
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805
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Comment: Comment: BIOINFORMATICS
17 months ago by Medhat 9.7k
2
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0
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907
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Comment: Comment: Looking for tools to individuate gene-gene correlations from a few candidates
17 months ago by Medhat 9.7k
0
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0
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1.0k
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Comment: Comment: No CR tag in the sam file mapped by STARsolo (10x v3.1 data)
17 months ago by Medhat 9.7k
0
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0
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1.8k
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Comment: Comment: Different results in finding human sequences from metagenomes (bowtie2 and Krake
18 months ago by Medhat 9.7k
0
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0
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1.2k
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Comment: Comment: bedtools intersect multiple files using for loop
18 months ago by Medhat 9.7k
1
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1
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1.2k
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Comment: Comment: bedtools intersect multiple files using for loop
18 months ago by Medhat 9.7k
0
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0
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928
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Comment: Comment: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Cen
19 months ago by Medhat 9.7k
0
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1
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928
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Job: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS TGS
updated 12 months ago by 44k • written 23 months ago by 9.7k
0
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1
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1.3k
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Comment: Comment: Introducing Cramino: a *fast* QC tool for long reads
19 months ago by Medhat 9.7k
0
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1
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1.0k
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Comment: Comment: For loop RNA Sequencing alignment
20 months ago by Medhat 9.7k
2
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0
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1.3k
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Comment: Comment: sorting multiple .bam files in linux cluster
21 months ago by Medhat 9.7k
0
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0
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1.1k
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Comment: Comment: gosling.js and React 1.7+
21 months ago by Medhat 9.7k
0
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1
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1.1k
views
Comment: Comment: gosling.js and React 1.7+
21 months ago by Medhat 9.7k
1
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1
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1.2k
views
Comment: Comment: Leaky RNA
22 months ago by Medhat 9.7k
0
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0
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939
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Comment: Comment: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Seq
22 months ago by Medhat 9.7k
0
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1
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1.4k
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Comment: Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
23 months ago by Medhat 9.7k
0
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0
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876
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Comment: Comment: getting the coordinates of mapped regions from a bam file
23 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
23 months ago by Medhat 9.7k
0
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0
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1.3k
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Comment: Comment: Programming languages in industry
23 months ago by Medhat 9.7k
2
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1
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1.3k
views
Answer: Answer: Programming languages in industry
23 months ago by Medhat 9.7k
0
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1
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939
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Job: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS TGS
updated 12 months ago by 44k • written 23 months ago by 9.7k
4
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3
replies
3.0k
views
Split VCF file
vcf sequencing
written 7.4 years ago by 9.7k
0
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0
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1.0k
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Comment: Comment: Source of soft clipped reads from target sequencing
2.1 years ago by Medhat 9.7k
1
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0
replies
1.7k
views
Answer: Answer: VCF Statistics
2.1 years ago by Medhat 9.7k
0
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1
reply
609
views
Comment: Comment: Align chimpanzee genome
2.1 years ago by Medhat 9.7k
2
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2
replies
2.9k
views
Answer: Answer: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
2.1 years ago by Medhat 9.7k
0
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0
replies
1.0k
views
Job: Postdoctoral Fellow Pacific Northwest Research Institute (PNRI) in Seattle
variants NGS
updated 24 months ago by 44k • written 2.1 years ago by 9.7k
1
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0
replies
797
views
Comment: Comment: How to generate a bam file with reads of only a certain length?
2.1 years ago by Medhat 9.7k
1
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1
reply
797
views
Comment: Comment: How to generate a bam file with reads of only a certain length?
2.1 years ago by Medhat 9.7k
0
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0
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766
views
Comment: Comment: how to visulize structure variants
2.1 years ago by Medhat 9.7k
2
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1
reply
766
views
Answer: Answer: how to visulize structure variants
2.1 years ago by Medhat 9.7k
1
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2
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4.8k
views
Using PRINSEQ lite with zipped paired-end illumina reads
prinseq next-gen-sequencing quality-reads Illumina
updated 2.2 years ago by • 0 • written 9.8 years ago by 9.7k
0
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0
replies
1.0k
views
Comment: Comment: liftOver input file
2.3 years ago by Medhat 9.7k
1,009 results • Page 1 of 21
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