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Comment: Comment: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
18 hours ago by Medhat 9.7k
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980
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Comment: Comment: guppy basecaller giving error while basecalling
10 months ago by Medhat 9.7k
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626
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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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1.2k
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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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1.2k
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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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1.5k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
11 months ago by Medhat 9.7k
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695
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Comment: Comment: Variant calling analysis
11 months ago by Medhat 9.7k
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695
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Comment: Comment: Variant calling analysis
11 months ago by Medhat 9.7k
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535
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Comment: Comment: Do we have any disease specific SNVs database?
14 months ago by Medhat 9.7k
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4.9k
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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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1.6k
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Comment: Comment: GATK showing error of reference file index
14 months ago by Medhat 9.7k
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521
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Comment: Comment: Methods for downsampling coverage in a VCF
14 months ago by Medhat 9.7k
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913
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Comment: Comment: I have a reference genome explained by accession number instead of chromosome nu
15 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
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746
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Comment: Comment: BIOINFORMATICS
15 months ago by Medhat 9.7k
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867
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Comment: Comment: Looking for tools to individuate gene-gene correlations from a few candidates
16 months ago by Medhat 9.7k
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970
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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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901
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Comment: Comment: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Cen
17 months ago by Medhat 9.7k
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1.2k
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Comment: Comment: Introducing Cramino: a *fast* QC tool for long reads
18 months ago by Medhat 9.7k
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1
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939
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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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1.0k
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Comment: Comment: gosling.js and React 1.7+
20 months ago by Medhat 9.7k
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1.0k
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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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1.1k
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Comment: Comment: Leaky RNA
20 months ago by Medhat 9.7k
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915
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Comment: Comment: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Seq
21 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
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828
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Comment: Comment: getting the coordinates of mapped regions from a bam file
22 months ago by Medhat 9.7k
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1.3k
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Comment: Comment: Programming languages in industry
22 months ago by Medhat 9.7k
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1.3k
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Comment: Comment: Programming languages in industry
22 months ago by Medhat 9.7k
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937
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Comment: Comment: Source of soft clipped reads from target sequencing
23 months ago by Medhat 9.7k
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1
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581
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Comment: Comment: Align chimpanzee genome
24 months ago by Medhat 9.7k
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759
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Comment: Comment: How to generate a bam file with reads of only a certain length?
2.0 years ago by Medhat 9.7k
1
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1
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759
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Comment: Comment: How to generate a bam file with reads of only a certain length?
2.0 years ago by Medhat 9.7k
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713
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Comment: Comment: how to visulize structure variants
2.0 years ago by Medhat 9.7k
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0
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955
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Comment: Comment: liftOver input file
2.2 years ago by Medhat 9.7k
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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
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1.6k
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Comment: Comment: Select variants that exist in all samples from a merged VCF file using bcftools
2.3 years ago by Medhat 9.7k
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1
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1.6k
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Comment: Comment: Select variants that exist in all samples from a merged VCF file using bcftools
2.3 years ago by Medhat 9.7k
0
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1
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799
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Comment: Comment: Tool that finds direct DNA repeats with mismatches
2.7 years ago by Medhat 9.7k
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1.2k
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Comment: Comment: Pipeline version control system, pipeline storage
2.7 years ago by Medhat 9.7k
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0
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2.2k
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Comment: Comment: install R package
2.9 years ago by Medhat 9.7k
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1.5k
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Comment: Comment: error on extracting a snp from vcf file using bcftools
2.9 years ago by Medhat 9.7k
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1
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1.5k
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Comment: Comment: error on extracting a snp from vcf file using bcftools
2.9 years ago by Medhat 9.7k
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0
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992
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Comment: Comment: Bioinformatician
2.9 years ago by Medhat 9.7k
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1
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1.8k
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Comment: Comment: HISAT2 Genome indexing
3.0 years ago by Medhat 9.7k
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0
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955
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Comment: Comment: Why we have exons that start and end at the same coordinate?!
3.1 years ago by Medhat 9.7k
750 results • Page 1 of 15
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