Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
0
votes
0
replies
490
views
Comment: Comment: circlize R package to plot ecDNA
9 weeks ago by trausch ★ 1.9k
0
votes
0
replies
408
views
Answer: Answer: Using Delly/Pindel/breakdancer for Identifying Transgene Insertion Sites in Mous
6 months ago by trausch ★ 1.9k
1
vote
1
reply
901
views
Answer: Answer: SHAPEIT5 phasing
8 months ago by trausch ★ 1.9k
1
vote
1
reply
1.0k
views
Answer: Answer: somatic variant calling without matched normal in long-reads
8 months ago by trausch ★ 1.9k
0
votes
0
replies
599
views
Answer: Answer: Protocol to combine WGS with Nanopore for Structural Variant confirmation?
8 months ago by trausch ★ 1.9k
1
vote
0
replies
460
views
Answer: Answer: Can sangeranalyseR be changed to read SCF files?
11 months ago by trausch ★ 1.9k
0
votes
0
replies
1.6k
views
Answer: Answer: Off-target % for whole-exome sequencing panel
18 months ago by trausch ★ 1.9k
0
votes
1
reply
869
views
Answer: Answer: delly filter input file
19 months ago by trausch ★ 1.9k
0
votes
0
replies
748
views
Answer: Answer: Index genome not working in Tracy
24 months ago by trausch ★ 1.9k
2
votes
1
reply
1.0k
views
Answer: Answer: clarifying head-to-head and tail-to-tail inversions
2.2 years ago by trausch ★ 1.9k
0
votes
1
reply
777
views
Answer: Answer: Any good tools to generate newicks files for a large list of species?
2.4 years ago by trausch ★ 1.9k
0
votes
0
replies
1.6k
views
Answer: Answer: Understanding ABI Sanger File Format
2.4 years ago by trausch ★ 1.9k
0
votes
0
replies
1.9k
views
Answer: Answer: Het/Mixed Indel identification tools
2.5 years ago by trausch ★ 1.9k
0
votes
0
replies
2.3k
views
Answer: Answer: How can I download the VCF file of the 1000 genomes project with the population
2.7 years ago by trausch ★ 1.9k
1
vote
0
replies
739
views
Answer: Answer: Customisable DNA Read Simulation for Deleted Reads
2.7 years ago by trausch ★ 1.9k
4
votes
1
reply
772
views
Answer: Answer: Sanger Sequence Analysis
2.7 years ago by trausch ★ 1.9k
2
votes
0
replies
1.4k
views
Answer: Answer: Usability of depiction of individual reads in genome browser visualization
2.9 years ago by trausch ★ 1.9k
0
votes
0
replies
1.4k
views
Answer: Answer: Detection of heterozygous exon deletion by Sanger and Long-Range PCR
2.9 years ago by trausch ★ 1.9k
1
vote
0
replies
2.2k
views
Answer: Answer: Command-line alternative to Geneious assemble for Sanger sequencing data
2.9 years ago by trausch ★ 1.9k
1
vote
0
replies
1.5k
views
Answer: Answer: Analysis of .ab1 file from sanger sequencer in galaxy
2.9 years ago by trausch ★ 1.9k
3
votes
3
replies
1.2k
views
Answer: Answer: How many reads does Delly use for variant calling?
3.3 years ago by trausch ★ 1.9k
1
vote
0
replies
1.8k
views
Answer: Answer: How to filter delly variants?
3.3 years ago by trausch ★ 1.9k
1
vote
1
reply
1.7k
views
Answer: A: SARS Cov2 NGS data analysis pipeline
3.8 years ago by trausch ★ 1.9k
2
votes
1
reply
725
views
Answer: A: Is there a data set for next-generation sequencing and third-generation sequenci
3.8 years ago by trausch ★ 1.9k
0
votes
0
replies
1.2k
views
Comment: C: Structural variants detection from assembled genome from Nanopore sequence data
3.8 years ago by trausch ★ 1.9k
0
votes
2
replies
1.2k
views
Answer: A: Structural variants detection from assembled genome from Nanopore sequence data
3.8 years ago by trausch ★ 1.9k
1
vote
0
replies
1.4k
views
Answer: A: Sanger sequencing chromatogram aligned to reference gene
3.9 years ago by trausch ★ 1.9k
0
votes
0
replies
3.3k
views
Answer: A: How to parse a .fasta file in python ?
3.9 years ago by trausch ★ 1.9k
1
vote
1
reply
3.9k
views
Answer: A: What are the strands of structural variant breakpoints?
4.0 years ago by trausch ★ 1.9k
0
votes
0
replies
1.0k
views
Answer: A: 1000 Genome Project Structural Variants for Illumina
4.1 years ago by trausch ★ 1.9k
3
votes
1
reply
7.4k
views
Answer: A: Convert VCF dosage file into dosage only file
updated 4.2 years ago by 12k • written 7.3 years ago by ★ 1.9k
0
votes
1
reply
2.2k
views
Comment: C: How to compare Sanger Sequenced data to the reference sequence?
4.5 years ago by trausch ★ 1.9k
1
vote
1
reply
2.2k
views
Answer: A: How to compare Sanger Sequenced data to the reference sequence?
4.5 years ago by trausch ★ 1.9k
1
vote
0
replies
6.3k
views
Answer: A: Software to analyse mutations in sanger sequencing files
4.5 years ago by trausch ★ 1.9k
0
votes
0
replies
27k
views
Answer: A: Automated Primer-Blast like funcionnality
4.8 years ago by trausch ★ 1.9k
1
vote
0
replies
5.1k
views
Answer: A: how to estimate heterozygosity by sample from a multi-sample vcf file
4.8 years ago by trausch ★ 1.9k
0
votes
1
reply
7.6k
views
Comment: C: Explain the definition of DELLY output
4.9 years ago by trausch ★ 1.9k
2
votes
2
replies
7.6k
views
Answer: A: Explain the definition of DELLY output
4.9 years ago by trausch ★ 1.9k
2
votes
1
reply
15k
views
Answer: A: Where to get list of all Illumina adapters
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
2
votes
0
replies
3.3k
views
Answer: A: Illumina WES intervals file for coverage analysis?
4.9 years ago by trausch ★ 1.9k
7
votes
1
reply
5.6k
views
Answer: A: List of CNV (copy number variation) regions in the human genome
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
2
votes
1
reply
39k
views
Answer: A: hg38 annotation file (gtf) UCSC format
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
1
vote
3
replies
3.9k
views
Answer: A: Displaying somatic mutational signatures
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
0
votes
0
replies
7.2k
views
Answer: A: Salvage barcode undetermined reads from Illumina HiSeq 2500 2 x 100 bp pair-ende
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
0
votes
2
replies
3.3k
views
Comment: C: Extraction of SNPs from the 1000G vcf file for a set of regions
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
2
votes
1
reply
3.0k
views
Answer: A: updating vcf file from rsIDs of dbsnp138 to dbsnp144
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
0
votes
0
replies
8.2k
views
Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
1
vote
1
reply
2.2k
views
Answer: A: How to add the gene names on wormbase_genes BED file?
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
3
votes
1
reply
2.7k
views
Answer: C: Is it correct to merge TCGA mutation data from multiple centers
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
2
votes
1
reply
2.8k
views
Comment: C: Calculation of heterozygosity at multi allelic region from 1000 Genomes data
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.9k
181 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