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0
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2
replies
3.0k
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Comment: C: Difference between Rad-Seq and amplicon seq
8.3 years ago by CY ▴ 750
2
votes
8
replies
3.0k
views
Difference between Rad-Seq and amplicon seq
amplicon sequencing rad-seq SNP next-gen
8.3 years ago by CY ▴ 750
3
votes
2
replies
1.6k
views
Detecting CNV can't cover aneuploidy situation
cnv next-gen sequence
updated 8.3 years ago by 48k • written 8.3 years ago by ▴ 750
2
votes
1
reply
1.7k
views
Best approach to quantify specific bacteria strain
qpcr snp sequence alignment
8.3 years ago by CY ▴ 750
0
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1
reply
1.4k
views
RAM / cache usage in frequently use BI pipeline
RNA-Seq SNP alignment next-gen
8.3 years ago by CY ▴ 750
0
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0
replies
12k
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Comment: C: STAR genomeLoad issue
8.3 years ago by CY ▴ 750
0
votes
1
reply
2.4k
views
Comment: C: What makes low frequency variants callers good at what they do?
8.3 years ago by CY ▴ 750
4
votes
5
replies
1.8k
views
Distributed / parallel computing in bioinformatics
distributed-computing
updated 2.5 years ago by 45k • written 8.3 years ago by ▴ 750
3
votes
3
replies
2.4k
views
What makes low frequency variants callers good at what they do?
variant calling LoFreq FreeBayes somatic mutation
8.3 years ago by CY ▴ 750
0
votes
1
reply
12k
views
Comment: C: STAR genomeLoad issue
8.3 years ago by CY ▴ 750
0
votes
1
reply
12k
views
Comment: C: STAR genomeLoad issue
8.3 years ago by CY ▴ 750
8
votes
15
replies
12k
views
6 follow
STAR genomeLoad issue
RNA-Seq
updated 8.3 years ago by 35k • written 8.3 years ago by ▴ 750
0
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0
replies
2.4k
views
Comment: C: Somatic variant caller
8.6 years ago by CY ▴ 750
1
vote
1
reply
2.0k
views
Distribution of somatic mutation
next-gen SNP
updated 8.6 years ago by ▴ 90 • written 8.6 years ago by ▴ 750
0
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0
replies
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
0
votes
1
reply
2.9k
views
Comment: C: Detecting variants at very low fractions from ctDNA
9.0 years ago by CY ▴ 750
3
votes
4
replies
2.9k
views
Detecting variants at very low fractions from ctDNA
ctDNA variants mutation
updated 9.0 years ago by ▴ 480 • written 9.0 years ago by ▴ 750
0
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0
replies
2.3k
views
Comment: C: 11% mutation frequency of TP53 in non-cancer samples
9.0 years ago by CY ▴ 750
0
votes
1
reply
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
0
votes
0
replies
1.2k
views
RNA expression profile for tumor sample OVER TIME
RNA-Seq tumor expression
9.0 years ago by CY ▴ 750
0
votes
1
reply
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
0
votes
0
replies
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
0
votes
0
replies
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
0
votes
1
reply
6.2k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
9.0 years ago by CY ▴ 750
6
votes
13
replies
6.2k
views
Call variant from RNA-Seq data using Haplotypecaller
RNA-Seq variant call GATK
updated 9.0 years ago by 6.7k • written 9.0 years ago by ▴ 750
2
votes
6
replies
1.9k
views
why GATK generates more SNP than samtool does
SNP next-gen sequencing
9.5 years ago by CY ▴ 750
0
votes
0
replies
1.2k
views
How genomic positions are selected for genetic testing
snp
updated 3.2 years ago by 45k • written 10.0 years ago by ▴ 750
0
votes
0
replies
1.2k
views
where can I find breast cancer risk loci (genomic coodinate) for BRCA gene
gene SNP
updated 3.2 years ago by 45k • written 10.0 years ago by ▴ 750
278 results • Page 6 of 6
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