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VEP cache trancript versions
annotation ngs dna-seq vep sequencing written 5 days ago by Chadi Saad • 70 • updated 2 days ago by Michal @Ensembl • 20
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targeted DNA sequencing
next-gen alignment dna-seq targeted sequencing written 5 days ago by Pettorato • 0
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News: NGS Data Analysis Trainings (Classroom and Online)
news dna-seq rna-seq training written 5 days ago by David Langenberger ♦ 9.5k
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News: A Practical Introduction to NGS Data Analysis - America Online Edition
ngs dna-seq news workshop written 16 days ago by David Langenberger ♦ 9.5k
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News: 4th Berlin Summer School in NGS Data Analysis - October 5-9, 2020
ngs dna-seq news rna-seq written 4 months ago by David Langenberger ♦ 9.5k
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know sites of rice for BaseRecalibrator
dna-seq written 3 months ago by 543541656 • 20
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DNA-Seq and Whole Genome Sequencing, are they the same?
genome dna-seq whole genome sequencing written 3 months ago by rtyb91 • 20 • updated 3 months ago by ATpoint ♦ 36k
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there is an error after samtools index
dna-seq written 3 months ago by 543541656 • 20 • updated 3 months ago by swbarnes2 ♦ 7.9k
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creating rarefaction curves
R metagenomics dna-seq written 6.0 years ago by Phil S. • 660 • updated 3 months ago by h.mon ♦ 30k
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115
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Extracting variant reads and reference reads quickly from mapped files
dna-seq variant written 3 months ago by graeme.thorn • 50
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Long-read alignment with Minimap2
minimap2 long-read dna-seq written 13 months ago by gokberk • 60 • updated 3 months ago by Biostar ♦♦ 20
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Heatmap value gradient
bioinformatics dna-seq R genomics heatmap written 4 months ago by ngcatung0 • 20 • updated 4 months ago by ashish • 430
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Want to edit bioperl script for making .ptt files (for each contig) from .gbk files.
genome software error dna-seq perl python written 6 months ago by Bioinfo_learner • 20 • updated 5 months ago by genomax ♦ 85k
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Job: Bioinformatician Positions at the University of Chicago BSD Bioinformatics Core
atac-seq proteomics job rna-seq microbiome dna-seq written 6 months ago by lhuang7 • 0 • updated 5 months ago by fu_entomology • 20
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Converting gff hints to genbank format for augustus training
augustus genome annotation dna-seq written 11 months ago by praasu • 30 • updated 6 months ago by marcos.a.godoy.f • 10
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Normalizing gene counts in a quantitative metagenomic DNAseq analysis
illumina dna-seq count depth written 7 months ago by allerdrengen55 • 20
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Why does BWA sometimes omit X0 and X1 tags?
burrows-wheeler aligner alignment dna-seq bwa written 7 months ago by b10hazard • 30 • updated 7 months ago by h.mon ♦ 30k
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Annotating dbnsfp by SnpSift on a cluster
snpsift annotation next-gen dna-seq dbnsfp written 8 months ago by kanika.151 • 80
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Which aligners are commonly used for DNA-seq data alignment?
dna-seq alignment sequencing written 8 months ago by manojkumar_bhosale • 70
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kraken2 different bacteria read counts on custom database
kraken2 metagenomics dna-seq written 13 months ago by bangbangphil2 • 0 • updated 8 months ago by ilyzdd • 10
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News: FINAL CALL - 'Introduction to NGS Data Analysis' course in Munich, October 23 - 25
news dna-seq ngs rna-seq workshop written 10 months ago by David Langenberger ♦ 9.5k
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Consensus reads from UMIs
umi dna-seq deduplication written 10 months ago by graeme.thorn • 50 • updated 10 months ago by finswimmer ♦ 13k
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From per bp coverage to average coverage in 10bp intervals
genome dna-seq bam written 11 months ago by Adrian Pelin • 2.4k • updated 11 months ago by Alex Reynolds ♦ 30k
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BWA mapping parameters for DNA capture sequencing protocol
alignment dna-seq bwa capture written 11 months ago by graeme.thorn • 50
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Are there any tools that can extract somatic variants from matched normal tumor vcf files?
variant calling ngs dna-seq written 11 months ago by Sandeep • 260 • updated 11 months ago by Kevin Blighe ♦ 61k
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Measure of SV genomic diversity in a population
structural variants dna-seq population genetics written 11 months ago by lucas.lochovsky • 0
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5 follow
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Forum: To Cloud or Not to Cloud - Privacy implications of genetic data sharing
forum dna-seq security diagnostics written 12 months ago by David Langenberger ♦ 9.5k • updated 12 months ago by anneykim • 0
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Filtering human reads in metagenomics: should supplementary reads be removed?
flagstat metagenomics dna-seq samtools bwa written 12 months ago by ciemanek • 140
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Blog: NGS-based research, empowering medical professionals through user-friendly software
illumina ngs dna-seq blog diagnostics written 16 months ago by David Langenberger ♦ 9.5k
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raw sequencing data
database dna-seq raw data sequencing written 14 months ago by Tasneem Fetian • 0 • updated 14 months ago by ATpoint ♦ 36k
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