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Comment: Comment: Visualise duplications and inversions
9 weeks ago by Medhat 9.8k
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947
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Comment: Comment: Install PacBio lima via conda fails
8 months ago by Medhat 9.8k
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1
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727
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Comment: Comment: Filtering the vcf file
8 months ago by Medhat 9.8k
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1.2k
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Comment: Comment: Variant Analyst Opening in Qatar
8 months ago by Medhat 9.8k
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3.8k
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Comment: Comment: How to download a file from zenodo link without leaving terminal?
12 months ago by Medhat 9.8k
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5.4k
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Comment: Comment: When to use .vcf or .gvcf files from GATK HaplotypeCaller?
13 months ago by Medhat 9.8k
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1.5k
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Comment: Comment: guppy basecaller giving error while basecalling
24 months ago by Medhat 9.8k
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1.2k
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Comment: Comment: More Efficient: Whole Genome VCF splitting with and without tbi file
2.0 years ago by Medhat 9.8k
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2.4k
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Comment: Comment: What are your preferred programs for processing DNA long reads? (de novo assembl
2.0 years ago by Medhat 9.8k
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2.1k
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Comment: Comment: Why some insertions are symbolic in ALT column?
2.0 years ago by Medhat 9.8k
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1
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2.5k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
2.1 years ago by Medhat 9.8k
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1
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2.5k
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Comment: Comment: Problem with GPU guppy_basecaller and SLURM
2.1 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: Variant calling analysis
2.1 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: Variant calling analysis
2.1 years ago by Medhat 9.8k
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1.0k
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Comment: Comment: Do we have any disease specific SNVs database?
2.3 years ago by Medhat 9.8k
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11k
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Comment: Comment: conda create env using .yml file leads to dependency conflicts
2.3 years ago by Medhat 9.8k
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1
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2.6k
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Comment: Comment: GATK showing error of reference file index
2.3 years ago by Medhat 9.8k
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1.0k
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Comment: Comment: Methods for downsampling coverage in a VCF
2.4 years ago by Medhat 9.8k
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1
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1.4k
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Comment: Comment: I have a reference genome explained by accession number instead of chromosome nu
2.4 years ago by Medhat 9.8k
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2
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4.3k
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Comment: Comment: SV calling using giraffe/vg
2.4 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: BIOINFORMATICS
2.4 years ago by Medhat 9.8k
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1.4k
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Comment: Comment: Looking for tools to individuate gene-gene correlations from a few candidates
2.5 years ago by Medhat 9.8k
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1.5k
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Comment: Comment: No CR tag in the sam file mapped by STARsolo (10x v3.1 data)
2.5 years ago by Medhat 9.8k
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2.7k
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Comment: Comment: Different results in finding human sequences from metagenomes (bowtie2 and Krake
2.5 years ago by Medhat 9.8k
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1.8k
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Comment: Comment: bedtools intersect multiple files using for loop
2.6 years ago by Medhat 9.8k
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1
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1.8k
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Comment: Comment: bedtools intersect multiple files using for loop
2.6 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: Postdoctoral Associate , Baylor College of Medicine, Human Genome Sequencing Cen
2.6 years ago by Medhat 9.8k
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1
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2.1k
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Comment: Comment: Introducing Cramino: a *fast* QC tool for long reads
2.6 years ago by Medhat 9.8k
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1
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1.7k
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Comment: Comment: For loop RNA Sequencing alignment
2.7 years ago by Medhat 9.8k
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1.8k
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Comment: Comment: sorting multiple .bam files in linux cluster
2.8 years ago by Medhat 9.8k
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1.6k
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Comment: Comment: gosling.js and React 1.7+
2.8 years ago by Medhat 9.8k
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1
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1.6k
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Comment: Comment: gosling.js and React 1.7+
2.8 years ago by Medhat 9.8k
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1
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1.8k
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Comment: Comment: Leaky RNA
2.8 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Seq
2.9 years ago by Medhat 9.8k
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1
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2.4k
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Comment: Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
2.9 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: getting the coordinates of mapped regions from a bam file
3.0 years ago by Medhat 9.8k
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2.1k
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Comment: Comment: Programming languages in industry
3.0 years ago by Medhat 9.8k
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2.1k
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Comment: Comment: Programming languages in industry
3.0 years ago by Medhat 9.8k
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1.6k
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Comment: Comment: Source of soft clipped reads from target sequencing
3.1 years ago by Medhat 9.8k
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1
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1.0k
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Comment: Comment: Align chimpanzee genome
3.1 years ago by Medhat 9.8k
1
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1.2k
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Comment: Comment: How to generate a bam file with reads of only a certain length?
3.1 years ago by Medhat 9.8k
1
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1
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1.2k
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Comment: Comment: How to generate a bam file with reads of only a certain length?
3.1 years ago by Medhat 9.8k
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1.2k
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Comment: Comment: how to visulize structure variants
3.2 years ago by Medhat 9.8k
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1.3k
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Comment: Comment: liftOver input file
3.3 years ago by Medhat 9.8k
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2.2k
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Comment: Comment: How to extract reads that support the structural variants using the vcf file and
3.4 years ago by Medhat 9.8k
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2.2k
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Comment: Comment: Select variants that exist in all samples from a merged VCF file using bcftools
3.5 years ago by Medhat 9.8k
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1
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2.2k
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Comment: Comment: Select variants that exist in all samples from a merged VCF file using bcftools
3.5 years ago by Medhat 9.8k
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1
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1.1k
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Comment: Comment: Tool that finds direct DNA repeats with mismatches
3.8 years ago by Medhat 9.8k
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0
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1.6k
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Comment: Comment: Pipeline version control system, pipeline storage
3.8 years ago by Medhat 9.8k
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0
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2.9k
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Comment: Comment: install R package
4.0 years ago by Medhat 9.8k
755 results • Page 1 of 16
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