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0
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2
replies
2.5k
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Comment: C: Difference between Rad-Seq and amplicon seq
7.4 years ago by CY ▴ 750
2
votes
8
replies
2.5k
views
Difference between Rad-Seq and amplicon seq
amplicon sequencing rad-seq SNP next-gen
7.4 years ago by CY ▴ 750
3
votes
2
replies
1.3k
views
Detecting CNV can't cover aneuploidy situation
cnv next-gen sequence
updated 7.4 years ago by 47k • written 7.4 years ago by ▴ 750
2
votes
1
reply
1.5k
views
Best approach to quantify specific bacteria strain
qpcr snp sequence alignment
7.5 years ago by CY ▴ 750
0
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1
reply
1.2k
views
RAM / cache usage in frequently use BI pipeline
RNA-Seq SNP alignment next-gen
7.5 years ago by CY ▴ 750
0
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0
replies
10k
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Comment: C: STAR genomeLoad issue
7.5 years ago by CY ▴ 750
0
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1
reply
2.0k
views
Comment: C: What makes low frequency variants callers good at what they do?
7.5 years ago by CY ▴ 750
4
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5
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1.5k
views
Distributed / parallel computing in bioinformatics
distributed-computing
updated 19 months ago by 44k • written 7.5 years ago by ▴ 750
3
votes
3
replies
2.0k
views
What makes low frequency variants callers good at what they do?
variant calling LoFreq FreeBayes somatic mutation
7.5 years ago by CY ▴ 750
0
votes
1
reply
10k
views
Comment: C: STAR genomeLoad issue
7.5 years ago by CY ▴ 750
0
votes
1
reply
10k
views
Comment: C: STAR genomeLoad issue
7.5 years ago by CY ▴ 750
8
votes
15
replies
10k
views
6 follow
STAR genomeLoad issue
RNA-Seq
updated 7.5 years ago by 35k • written 7.5 years ago by ▴ 750
0
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0
replies
2.1k
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Comment: C: Somatic variant caller
7.8 years ago by CY ▴ 750
1
vote
1
reply
1.8k
views
Distribution of somatic mutation
next-gen SNP
updated 7.8 years ago by ▴ 90 • written 7.8 years ago by ▴ 750
0
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0
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5.5k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
0
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1
reply
2.5k
views
Comment: C: Detecting variants at very low fractions from ctDNA
8.1 years ago by CY ▴ 750
3
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4
replies
2.5k
views
Detecting variants at very low fractions from ctDNA
ctDNA variants mutation
updated 8.1 years ago by ▴ 480 • written 8.1 years ago by ▴ 750
0
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0
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1.9k
views
Comment: C: 11% mutation frequency of TP53 in non-cancer samples
8.1 years ago by CY ▴ 750
0
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1
reply
5.5k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
0
votes
0
replies
1.1k
views
RNA expression profile for tumor sample OVER TIME
RNA-Seq tumor expression
8.1 years ago by CY ▴ 750
0
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1
reply
5.5k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
0
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0
replies
5.5k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
0
votes
0
replies
5.5k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
0
votes
1
reply
5.5k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.1 years ago by CY ▴ 750
6
votes
13
replies
5.5k
views
Call variant from RNA-Seq data using Haplotypecaller
RNA-Seq variant call GATK
updated 8.2 years ago by 6.6k • written 8.2 years ago by ▴ 750
2
votes
6
replies
1.6k
views
why GATK generates more SNP than samtool does
SNP next-gen sequencing
8.7 years ago by CY ▴ 750
0
votes
0
replies
1.1k
views
How genomic positions are selected for genetic testing
snp
updated 2.3 years ago by 44k • written 9.1 years ago by ▴ 750
0
votes
0
replies
1.1k
views
where can I find breast cancer risk loci (genomic coodinate) for BRCA gene
gene SNP
updated 2.3 years ago by 44k • written 9.1 years ago by ▴ 750
278 results • Page 6 of 6
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