Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
0
votes
0
replies
821
views
Answer: Answer: Off-target % for whole-exome sequencing panel
6 months ago by trausch ★ 1.8k
0
votes
1
reply
558
views
Answer: Answer: delly filter input file
8 months ago by trausch ★ 1.8k
0
votes
0
replies
546
views
Answer: Answer: Index genome not working in Tracy
12 months ago by trausch ★ 1.8k
2
votes
1
reply
597
views
Answer: Answer: clarifying head-to-head and tail-to-tail inversions
14 months ago by trausch ★ 1.8k
0
votes
1
reply
519
views
Answer: Answer: Any good tools to generate newicks files for a large list of species?
17 months ago by trausch ★ 1.8k
0
votes
0
replies
941
views
Answer: Answer: Understanding ABI Sanger File Format
17 months ago by trausch ★ 1.8k
0
votes
0
replies
1.7k
views
Answer: Answer: Het/Mixed Indel identification tools
18 months ago by trausch ★ 1.8k
0
votes
0
replies
1.6k
views
Answer: Answer: How can I download the VCF file of the 1000 genomes project with the population
21 months ago by trausch ★ 1.8k
1
vote
0
replies
518
views
Answer: Answer: Customisable DNA Read Simulation for Deleted Reads
21 months ago by trausch ★ 1.8k
4
votes
1
reply
537
views
Answer: Answer: Sanger Sequence Analysis
21 months ago by trausch ★ 1.8k
2
votes
0
replies
1.0k
views
Answer: Answer: Usability of depiction of individual reads in genome browser visualization
23 months ago by trausch ★ 1.8k
0
votes
0
replies
1.0k
views
Answer: Answer: Detection of heterozygous exon deletion by Sanger and Long-Range PCR
24 months ago by trausch ★ 1.8k
1
vote
0
replies
1.7k
views
Answer: Answer: Command-line alternative to Geneious assemble for Sanger sequencing data
24 months ago by trausch ★ 1.8k
1
vote
0
replies
1.1k
views
Answer: Answer: Analysis of .ab1 file from sanger sequencer in galaxy
24 months ago by trausch ★ 1.8k
3
votes
3
replies
864
views
Answer: Answer: How many reads does Delly use for variant calling?
2.4 years ago by trausch ★ 1.8k
1
vote
0
replies
1.5k
views
Answer: Answer: How to filter delly variants?
2.4 years ago by trausch ★ 1.8k
1
vote
1
reply
1.4k
views
Answer: A: SARS Cov2 NGS data analysis pipeline
2.9 years ago by trausch ★ 1.8k
2
votes
1
reply
585
views
Answer: A: Is there a data set for next-generation sequencing and third-generation sequenci
2.9 years ago by trausch ★ 1.8k
0
votes
0
replies
912
views
Comment: C: Structural variants detection from assembled genome from Nanopore sequence data
2.9 years ago by trausch ★ 1.8k
0
votes
2
replies
912
views
Answer: A: Structural variants detection from assembled genome from Nanopore sequence data
2.9 years ago by trausch ★ 1.8k
1
vote
0
replies
1.1k
views
Answer: A: Sanger sequencing chromatogram aligned to reference gene
2.9 years ago by trausch ★ 1.8k
0
votes
0
replies
2.7k
views
Answer: A: How to parse a .fasta file in python ?
2.9 years ago by trausch ★ 1.8k
1
vote
1
reply
3.3k
views
Answer: A: What are the strands of structural variant breakpoints?
3.0 years ago by trausch ★ 1.8k
0
votes
0
replies
805
views
Answer: A: 1000 Genome Project Structural Variants for Illumina
3.2 years ago by trausch ★ 1.8k
3
votes
1
reply
6.8k
views
Answer: A: Convert VCF dosage file into dosage only file
updated 3.3 years ago by 11k • written 6.4 years ago by ★ 1.8k
0
votes
1
reply
1.6k
views
Comment: C: How to compare Sanger Sequenced data to the reference sequence?
3.6 years ago by trausch ★ 1.8k
1
vote
1
reply
1.6k
views
Answer: A: How to compare Sanger Sequenced data to the reference sequence?
3.6 years ago by trausch ★ 1.8k
1
vote
0
replies
5.6k
views
Answer: A: Software to analyse mutations in sanger sequencing files
3.6 years ago by trausch ★ 1.8k
0
votes
0
replies
25k
views
Answer: A: Automated Primer-Blast like funcionnality
3.8 years ago by trausch ★ 1.8k
1
vote
0
replies
3.9k
views
Answer: A: how to estimate heterozygosity by sample from a multi-sample vcf file
3.8 years ago by trausch ★ 1.8k
0
votes
1
reply
6.5k
views
Comment: C: Explain the definition of DELLY output
3.9 years ago by trausch ★ 1.8k
2
votes
2
replies
6.5k
views
Answer: A: Explain the definition of DELLY output
3.9 years ago by trausch ★ 1.8k
2
votes
1
reply
14k
views
Answer: A: Where to get list of all Illumina adapters
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
2
votes
0
replies
2.7k
views
Answer: A: Illumina WES intervals file for coverage analysis?
3.9 years ago by trausch ★ 1.8k
7
votes
1
reply
5.4k
views
Answer: A: List of CNV (copy number variation) regions in the human genome
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
2
votes
1
reply
37k
views
Answer: A: hg38 annotation file (gtf) UCSC format
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
3
replies
3.6k
views
Answer: A: Displaying somatic mutational signatures
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
0
votes
0
replies
6.7k
views
Answer: A: Salvage barcode undetermined reads from Illumina HiSeq 2500 2 x 100 bp pair-ende
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
0
votes
2
replies
2.7k
views
Comment: C: Extraction of SNPs from the 1000G vcf file for a set of regions
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
2
votes
1
reply
2.7k
views
Answer: A: updating vcf file from rsIDs of dbsnp138 to dbsnp144
updated 3.9 years ago by 41k • written 7.9 years ago by ★ 1.8k
0
votes
0
replies
7.6k
views
Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
1
reply
2.0k
views
Answer: A: How to add the gene names on wormbase_genes BED file?
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
3
votes
1
reply
2.4k
views
Answer: C: Is it correct to merge TCGA mutation data from multiple centers
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
2
votes
1
reply
2.6k
views
Comment: C: Calculation of heterozygosity at multi allelic region from 1000 Genomes data
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
1
reply
8.9k
views
Answer: A: Proper way of calculating minor allele frequencies (via vcftools)
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
0
replies
9.4k
views
Comment: C: Spades assembler output
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
2
votes
0
replies
1.9k
views
Answer: A: Genome sequencing and depth of coverage
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
0
votes
0
replies
5.9k
views
Answer: A: How to score a multiple sequence alignment (MSA)?
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
0
replies
5.1k
views
Answer: A: Exploratory data anaylsis to detect batch effects
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
1
vote
0
replies
3.7k
views
Comment: C: Does anyone know any specific 1000 genomes WGS data that is around 30x coverage?
updated 4.0 years ago by 41k • written 7.9 years ago by ★ 1.8k
175 results • Page 1 of 4
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6