Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : answers
3
votes
1
reply
2.1k
views
Answer: Answer: What is your preferred annotation techniques when you analyze mutation in exome
updated 16 months ago by 43k • written 9.0 years ago by ▴ 860
0
votes
2
replies
3.4k
views
Answer: A: extract data from txt files
updated 4.5 years ago by 43k • written 8.7 years ago by ▴ 860
3
votes
1
reply
7.5k
views
Answer: A: How can you convert a GATK interval_list file into a BED file
updated 4.5 years ago by 43k • written 8.9 years ago by ▴ 860
1
vote
2
replies
1.8k
views
Answer: A: python newbie - only else statement is printed
7.4 years ago by Zaag ▴ 860
0
votes
1
reply
3.5k
views
Answer: A: Beginner at Python- My task is to convert a FASTA file to a PHYLIP file (tab-del
7.4 years ago by Zaag ▴ 860
1
vote
0
replies
2.3k
views
Answer: A: Where can I find NGS data to test alignment and SNP detection tool
7.5 years ago by Zaag ▴ 860
4
votes
1
reply
1.7k
views
Answer: A: Variant Calling problem - find alternate heterozygous
7.5 years ago by Zaag ▴ 860
2
votes
1
reply
2.7k
views
Answer: A: How can I get the exon number/rank of a mutation from annovar annotation?
7.5 years ago by Zaag ▴ 860
1
vote
0
replies
1.6k
views
Answer: A: use a input file to a mysql query to retrieve genomic coordinates from a list of
7.5 years ago by Zaag ▴ 860
0
votes
1
reply
2.2k
views
Answer: A: How to do context dependent data merge in python?
7.5 years ago by Zaag ▴ 860
0
votes
1
reply
6.0k
views
Answer: A: Rmarkdown report from multiple images
7.5 years ago by Zaag ▴ 860
1
vote
1
reply
7.9k
views
Answer: A: Learning Python: list of resources
7.5 years ago by Zaag ▴ 860
0
votes
1
reply
2.5k
views
Answer: A: IndelRealigner and RealignerTargetCreator for amplicon sequencing
7.5 years ago by Zaag ▴ 860
0
votes
0
replies
2.2k
views
Answer: A: Change vcf header in windows
7.6 years ago by Zaag ▴ 860
2
votes
1
reply
4.9k
views
Answer: A: Coverage analysis in a targeted amplicon-based next-generation sequencing panel
7.6 years ago by Zaag ▴ 860
0
votes
1
reply
2.9k
views
Answer: A: remove a percent of reads from a BAM file
7.7 years ago by Zaag ▴ 860
0
votes
1
reply
2.1k
views
Answer: A: Remove few samples and their related information from dbSNP
7.8 years ago by Zaag ▴ 860
1
vote
1
reply
1.6k
views
Answer: A: Number of private variants/singletons in identical twins
7.9 years ago by Zaag ▴ 860
1
vote
1
reply
3.8k
views
Answer: A: Large VCF QUAL Values
7.9 years ago by Zaag ▴ 860
0
votes
0
replies
6.4k
views
Answer: A: Does anyone use Python for variant calling?
7.9 years ago by Zaag ▴ 860
0
votes
1
reply
3.1k
views
Answer: A: What is best commercial software for exome/genome interpretation?
7.9 years ago by Zaag ▴ 860
0
votes
1
reply
10k
views
Answer: A: [Python] How to convert a list to a dictionary if dict() does not work without u
8.1 years ago by Zaag ▴ 860
2
votes
2
replies
1.9k
views
Answer: A: Python or shell scripting code ro count individual mapped reads of amplicons
8.1 years ago by Zaag ▴ 860
0
votes
0
replies
2.0k
views
Answer: A: Variant annotation tool
8.1 years ago by Zaag ▴ 860
2
votes
0
replies
2.7k
views
Answer: A: Perl help regarding hash
8.2 years ago by Zaag ▴ 860
0
votes
0
replies
2.2k
views
Answer: A: Nextseq 500 sample exome data
8.3 years ago by Zaag ▴ 860
1
vote
0
replies
6.5k
views
Answer: A: Fisher Strand in GATK, a good measure to detect Strand Bias?
8.5 years ago by Zaag ▴ 860
1
vote
0
replies
4.9k
views
Answer: Answer: Showing both strands in IGV, or if not possible what genome viewer is good for s
updated 20 months ago by 43k • written 8.6 years ago by ▴ 860
0
votes
0
replies
4.4k
views
Answer: Answer: variant calling on amplicon data
updated 19 months ago by 43k • written 8.7 years ago by ▴ 860
0
votes
1
reply
9.4k
views
Answer: Answer: Bait/Target files for Picard HsMetrics (Exome Sequencing)
updated 19 months ago by 43k • written 8.7 years ago by ▴ 860
2
votes
0
replies
4.6k
views
Answer: Answer: GATK IndelRealigner issue "TOO MANY READS"
updated 16 months ago by 43k • written 8.9 years ago by ▴ 860
2
votes
0
replies
2.0k
views
Answer: A: Good tool for viewing Multiallelic vcf/bcf files
8.9 years ago by Zaag ▴ 860
4
votes
1
reply
3.2k
views
Answer: Answer: Whole Genome Sequence (WGS) throughput (FastQC, Picard)
updated 16 months ago by 43k • written 8.9 years ago by ▴ 860
2
votes
0
replies
3.5k
views
Answer: Answer: Questions regarding proprocess for raw data and usage of FastQC
updated 16 months ago by 43k • written 8.9 years ago by ▴ 860
0
votes
0
replies
1.3k
views
Answer: Answer: Exome Sequencing Resources
updated 3.0 years ago by 43k • written 9.0 years ago by ▴ 860
0
votes
0
replies
3.7k
views
Answer: Answer: Alternatives to LifeScope for realigning SOLiD BAM files
updated 22 months ago by 43k • written 9.0 years ago by ▴ 860
0
votes
0
replies
2.6k
views
Answer: A: Variant Analysis on MiSeq Data
9.1 years ago by Zaag ▴ 860
3
votes
2
replies
17k
views
Answer: Answer: shell script for bowtie/bwa alignment pair end reads
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 860
0
votes
1
reply
3.0k
views
Answer: A: How long does it usually take to process exome sequencing samples with GATK's Un
10.0 years ago by Zaag ▴ 860
39 results • Page 1 of 1
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