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26
votes
21
replies
12k
views
13 follow
Tool for random access to indexed BAM files in S3?
BAM
cloud
updated 22 months ago by
Ram
44k • written 9.4 years ago by
donfreed
★ 1.6k
1
vote
0
replies
4.1k
views
Answer:
A: gVCF files from 1000 Genomes samples
4.1 years ago by
donfreed
★ 1.6k
16
votes
4
replies
4.1k
views
gVCF files from 1000 Genomes samples
gvcf
1000 Genomes
4.1 years ago by
donfreed
★ 1.6k
1
vote
1
reply
1.0k
views
Answer:
A: Error-prone human genomic sequence data from Illumina sequencing platform
4.3 years ago by
donfreed
★ 1.6k
1
vote
0
replies
2.9k
views
Answer:
A: Pipeline for analysing multiple tumor/normal exome samples
updated 4.8 years ago by
Ram
44k • written 10.4 years ago by
donfreed
★ 1.6k
0
votes
0
replies
2.4k
views
Answer:
A: Identifying mutations from Paired-End Sequencing data
updated 4.9 years ago by
Ram
44k • written 10.5 years ago by
donfreed
★ 1.6k
0
votes
0
replies
2.4k
views
Answer:
A: Genotype Calling
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
donfreed
★ 1.6k
2
votes
0
replies
2.6k
views
Answer:
A: Coding postions for genes in RefSeq
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
donfreed
★ 1.6k
0
votes
1
reply
6.2k
views
Answer:
A: CNVnator installation error
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
donfreed
★ 1.6k
3
votes
2
replies
3.6k
views
Answer:
A: Can germline vs somatic variants be distinguished by phasing when no control is
updated 4.9 years ago by
Ram
44k • written 8.9 years ago by
donfreed
★ 1.6k
0
votes
0
replies
3.6k
views
Comment:
C: Can germline vs somatic variants be distinguished by phasing when no control is
updated 4.9 years ago by
Ram
44k • written 8.9 years ago by
donfreed
★ 1.6k
45
votes
2
replies
59k
views
Answer:
A: What are chimeric reads?
updated 5.1 years ago by
Ram
44k • written 10.1 years ago by
donfreed
★ 1.6k
0
votes
0
replies
7.4k
views
Comment:
C: Modifying fasta file based on vcf information
6.7 years ago by
donfreed
★ 1.6k
0
votes
0
replies
3.4k
views
Comment:
C: how to distinguish mosaicism out of germline de novo mutations
6.7 years ago by
donfreed
★ 1.6k
3
votes
1
reply
3.4k
views
Answer:
A: how to distinguish mosaicism out of germline de novo mutations
6.8 years ago by
donfreed
★ 1.6k
1
vote
0
replies
4.1k
views
Answer:
A: Mutect 2 on WGS data takes too long to run
7.2 years ago by
donfreed
★ 1.6k
1
vote
1
reply
3.6k
views
Answer:
A: How to find variants that are common in one population but rare in others (popul
7.9 years ago by
donfreed
★ 1.6k
1
vote
1
reply
3.0k
views
Comment:
C: I want to store a docker image reproducing a paper. Is there a host for docker i
8.3 years ago by
donfreed
★ 1.6k
2
votes
1
reply
4.1k
views
Comment:
C: gVCF files from 1000 Genomes samples
8.4 years ago by
donfreed
★ 1.6k
2
votes
0
replies
2.3k
views
Answer:
Answer: A command line option for region in GenotypeGVCFs?
updated 2.3 years ago by
Ram
44k • written 8.7 years ago by
donfreed
★ 1.6k
1
vote
0
replies
1.8k
views
Answer:
A: Algorithm to find PL indicies containing a specific allele
8.8 years ago by
donfreed
★ 1.6k
1
vote
1
reply
1.8k
views
Algorithm to find PL indicies containing a specific allele
VCF
sequencing
algorithm
updated 2.3 years ago by
Ram
44k • written 8.8 years ago by
donfreed
★ 1.6k
0
votes
0
replies
2.7k
views
Comment:
C: Calculation of PFBs for CNV analysis from 1000 Genomes data
9.0 years ago by
donfreed
★ 1.6k
1
vote
1
reply
12k
views
Comment:
Comment: Tool for random access to indexed BAM files in S3?
updated 2.2 years ago by
Ram
44k • written 9.0 years ago by
donfreed
★ 1.6k
2
votes
2
replies
12k
views
Comment:
Comment: Tool for random access to indexed BAM files in S3?
updated 2.2 years ago by
Ram
44k • written 9.1 years ago by
donfreed
★ 1.6k
0
votes
0
replies
2.5k
views
Comment:
Comment: 1000 genomes technical data: match exon capture probes to samples
updated 2.1 years ago by
Ram
44k • written 9.2 years ago by
donfreed
★ 1.6k
0
votes
1
reply
12k
views
Comment:
C: Tool for random access to indexed BAM files in S3?
9.4 years ago by
donfreed
★ 1.6k
2
votes
0
replies
12k
views
Comment:
C: Tool for random access to indexed BAM files in S3?
9.4 years ago by
donfreed
★ 1.6k
0
votes
2
replies
2.7k
views
Calculation of PFBs for CNV analysis from 1000 Genomes data
snp
microarry
sequencing
penncnv
updated 9.4 years ago by
Biostar
20 • written 10.5 years ago by
donfreed
★ 1.6k
0
votes
0
replies
2.3k
views
Comment:
Comment: No more hidden solutions in bioinformatics
updated 21 months ago by
Ram
44k • written 9.5 years ago by
donfreed
★ 1.6k
0
votes
1
reply
6.8k
views
Comment:
C: bwa mem runs slowly the first time
9.5 years ago by
donfreed
★ 1.6k
0
votes
1
reply
6.8k
views
Comment:
Comment: bwa mem runs slowly the first time
updated 21 months ago by
Ram
44k • written 9.5 years ago by
donfreed
★ 1.6k
0
votes
1
reply
6.8k
views
Answer:
A: bwa mem runs slowly the first time
9.5 years ago by
donfreed
★ 1.6k
6
votes
0
replies
4.4k
views
Answer:
Answer: Phasing trios for identification of denovo variants
updated 21 months ago by
Ram
44k • written 9.5 years ago by
donfreed
★ 1.6k
0
votes
1
reply
5.9k
views
Comment:
C: dbGaP, error downloading files
9.6 years ago by
donfreed
★ 1.6k
1
vote
1
reply
4.4k
views
Answer:
A: What are most recommended / state-of-the-art whole genome FASTQ datasets for ben
9.6 years ago by
donfreed
★ 1.6k
0
votes
0
replies
3.6k
views
Answer:
Answer: Unaligning BAM files
updated 2.5 years ago by
Ram
44k • written 9.7 years ago by
donfreed
★ 1.6k
1
vote
2
replies
13k
views
Comment:
Comment: bwa mem perfectly align reads over their entire length
updated 2.5 years ago by
Ram
44k • written 9.7 years ago by
donfreed
★ 1.6k
2
votes
0
replies
3.4k
views
Answer:
Answer: Getting started with NGS analysis, common issues?
updated 2.5 years ago by
Ram
44k • written 9.7 years ago by
donfreed
★ 1.6k
3
votes
1
reply
3.2k
views
Answer:
Answer: Get Reference file from BAM
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
donfreed
★ 1.6k
5
votes
0
replies
8.2k
views
Answer:
Answer: Validated CNV dataset for NA12878
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
donfreed
★ 1.6k
1
vote
1
reply
1.6k
views
Answer:
Answer: Dot mark in 1000 genome project
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
donfreed
★ 1.6k
2
votes
0
replies
4.0k
views
Answer:
Answer: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.7 years ago by
Ram
44k • written 10.0 years ago by
donfreed
★ 1.6k
1
vote
1
reply
4.0k
views
Comment:
Comment: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.7 years ago by
Ram
44k • written 10.0 years ago by
donfreed
★ 1.6k
0
votes
1
reply
4.0k
views
Comment:
Comment: What is appropriate coverage/quality filter for GATK for germline variants?
updated 2.7 years ago by
Ram
44k • written 10.0 years ago by
donfreed
★ 1.6k
4
votes
1
reply
59k
views
Comment:
C: What are chimeric reads?
10.1 years ago by
donfreed
★ 1.6k
5
votes
1
reply
6.3k
views
Answer:
Answer: Do freeBayes and platypus support gVCF (ie incremental variant calling for large
updated 2.8 years ago by
Ram
44k • written 10.1 years ago by
donfreed
★ 1.6k
7
votes
0
replies
143k
views
Answer:
Answer: from .BAM to .BAI using samtools
updated 2.8 years ago by
Ram
44k • written 10.1 years ago by
donfreed
★ 1.6k
4
votes
0
replies
5.7k
views
Answer:
Answer: Haplotype frequencies from 1000 genomes
updated 2.8 years ago by
Ram
44k • written 10.1 years ago by
donfreed
★ 1.6k
2
votes
0
replies
10.0k
views
Comment:
Comment: Is it possible to reconstruct alignment from CIGAR and MD strings alone?
updated 2.9 years ago by
Ram
44k • written 10.2 years ago by
donfreed
★ 1.6k
69 results • Page
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