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26
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Tool for random access to indexed BAM files in S3?
BAM cloud
updated 16 months ago by 43k • written 8.8 years ago by ★ 1.6k
1
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0
replies
3.8k
views
Answer: A: gVCF files from 1000 Genomes samples
3.5 years ago by donfreed ★ 1.6k
16
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4
replies
3.8k
views
gVCF files from 1000 Genomes samples
gvcf 1000 Genomes
3.5 years ago by donfreed ★ 1.6k
1
vote
1
reply
931
views
Answer: A: Error-prone human genomic sequence data from Illumina sequencing platform
3.7 years ago by donfreed ★ 1.6k
1
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0
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2.7k
views
Answer: A: Pipeline for analysing multiple tumor/normal exome samples
updated 4.3 years ago by 43k • written 9.9 years ago by ★ 1.6k
0
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0
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2.3k
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Answer: A: Identifying mutations from Paired-End Sequencing data
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.6k
0
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0
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2.3k
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Answer: A: Genotype Calling
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.6k
2
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0
replies
2.5k
views
Answer: A: Coding postions for genes in RefSeq
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 1.6k
0
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1
reply
5.9k
views
Answer: A: CNVnator installation error
updated 4.3 years ago by 43k • written 8.3 years ago by ★ 1.6k
3
votes
2
replies
3.4k
views
Answer: A: Can germline vs somatic variants be distinguished by phasing when no control is
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 1.6k
0
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0
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3.4k
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Comment: C: Can germline vs somatic variants be distinguished by phasing when no control is
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 1.6k
44
votes
2
replies
56k
views
Answer: A: What are chimeric reads?
updated 4.5 years ago by 43k • written 9.5 years ago by ★ 1.6k
0
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0
replies
7.0k
views
Comment: C: Modifying fasta file based on vcf information
6.2 years ago by donfreed ★ 1.6k
0
votes
0
replies
3.2k
views
Comment: C: how to distinguish mosaicism out of germline de novo mutations
6.2 years ago by donfreed ★ 1.6k
3
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1
reply
3.2k
views
Answer: A: how to distinguish mosaicism out of germline de novo mutations
6.2 years ago by donfreed ★ 1.6k
1
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0
replies
3.8k
views
Answer: A: Mutect 2 on WGS data takes too long to run
6.7 years ago by donfreed ★ 1.6k
1
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1
reply
3.4k
views
Answer: A: How to find variants that are common in one population but rare in others (popul
7.3 years ago by donfreed ★ 1.6k
1
vote
1
reply
2.6k
views
Comment: C: I want to store a docker image reproducing a paper. Is there a host for docker i
7.7 years ago by donfreed ★ 1.6k
2
votes
1
reply
3.8k
views
Comment: C: gVCF files from 1000 Genomes samples
7.9 years ago by donfreed ★ 1.6k
2
votes
0
replies
2.2k
views
Answer: Answer: A command line option for region in GenotypeGVCFs?
updated 21 months ago by 43k • written 8.2 years ago by ★ 1.6k
1
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0
replies
1.7k
views
Answer: A: Algorithm to find PL indicies containing a specific allele
8.2 years ago by donfreed ★ 1.6k
1
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1
reply
1.7k
views
Algorithm to find PL indicies containing a specific allele
VCF sequencing algorithm
updated 20 months ago by 43k • written 8.2 years ago by ★ 1.6k
0
votes
0
replies
2.6k
views
Comment: C: Calculation of PFBs for CNV analysis from 1000 Genomes data
8.4 years ago by donfreed ★ 1.6k
1
vote
1
reply
11k
views
Comment: Comment: Tool for random access to indexed BAM files in S3?
updated 20 months ago by 43k • written 8.4 years ago by ★ 1.6k
2
votes
2
replies
11k
views
Comment: Comment: Tool for random access to indexed BAM files in S3?
updated 19 months ago by 43k • written 8.6 years ago by ★ 1.6k
0
votes
0
replies
2.4k
views
Comment: Comment: 1000 genomes technical data: match exon capture probes to samples
updated 18 months ago by 43k • written 8.7 years ago by ★ 1.6k
0
votes
1
reply
11k
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Comment: C: Tool for random access to indexed BAM files in S3?
8.8 years ago by donfreed ★ 1.6k
2
votes
0
replies
11k
views
Comment: C: Tool for random access to indexed BAM files in S3?
8.8 years ago by donfreed ★ 1.6k
0
votes
2
replies
2.6k
views
Calculation of PFBs for CNV analysis from 1000 Genomes data
snp microarry sequencing penncnv
updated 8.8 years ago by 20 • written 9.9 years ago by ★ 1.6k
0
votes
0
replies
2.1k
views
Comment: Comment: No more hidden solutions in bioinformatics
updated 15 months ago by 43k • written 8.9 years ago by ★ 1.6k
0
votes
1
reply
6.4k
views
Comment: C: bwa mem runs slowly the first time
8.9 years ago by donfreed ★ 1.6k
0
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1
reply
6.4k
views
Comment: Comment: bwa mem runs slowly the first time
updated 14 months ago by 43k • written 8.9 years ago by ★ 1.6k
0
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1
reply
6.4k
views
Answer: A: bwa mem runs slowly the first time
8.9 years ago by donfreed ★ 1.6k
6
votes
0
replies
4.1k
views
Answer: Answer: Phasing trios for identification of denovo variants
updated 14 months ago by 43k • written 8.9 years ago by ★ 1.6k
0
votes
1
reply
5.6k
views
Comment: C: dbGaP, error downloading files
9.0 years ago by donfreed ★ 1.6k
1
vote
1
reply
4.1k
views
Answer: A: What are most recommended / state-of-the-art whole genome FASTQ datasets for ben
9.0 years ago by donfreed ★ 1.6k
0
votes
0
replies
3.3k
views
Answer: Answer: Unaligning BAM files
updated 23 months ago by 43k • written 9.1 years ago by ★ 1.6k
1
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2
replies
13k
views
Comment: Comment: bwa mem perfectly align reads over their entire length
updated 23 months ago by 43k • written 9.1 years ago by ★ 1.6k
2
votes
0
replies
3.2k
views
Answer: Answer: Getting started with NGS analysis, common issues?
updated 24 months ago by 43k • written 9.2 years ago by ★ 1.6k
3
votes
1
reply
3.1k
views
Answer: Answer: Get Reference file from BAM
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 1.6k
5
votes
0
replies
7.9k
views
Answer: Answer: Validated CNV dataset for NA12878
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 1.6k
1
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1
reply
1.5k
views
Answer: Answer: Dot mark in 1000 genome project
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 1.6k
2
votes
0
replies
3.8k
views
Answer: Answer: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.1 years ago by 43k • written 9.4 years ago by ★ 1.6k
1
vote
1
reply
3.8k
views
Comment: Comment: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.1 years ago by 43k • written 9.4 years ago by ★ 1.6k
0
votes
1
reply
3.8k
views
Comment: Comment: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.1 years ago by 43k • written 9.4 years ago by ★ 1.6k
4
votes
1
reply
56k
views
Comment: C: What are chimeric reads?
9.5 years ago by donfreed ★ 1.6k
5
votes
1
reply
6.1k
views
Answer: Answer: Do freeBayes and platypus support gVCF (ie incremental variant calling for large
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 1.6k
6
votes
0
replies
129k
views
Answer: Answer: from .BAM to .BAI using samtools
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 1.6k
4
votes
0
replies
5.4k
views
Answer: Answer: Haplotype frequencies from 1000 genomes
updated 2.2 years ago by 43k • written 9.5 years ago by ★ 1.6k
2
votes
0
replies
9.3k
views
Comment: Comment: Is it possible to reconstruct alignment from CIGAR and MD strings alone?
updated 2.3 years ago by 43k • written 9.6 years ago by ★ 1.6k
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