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1
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0
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3.4k
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Comment: C: Rare Variants Study Using Next-Gen Sequencing Data
12.4 years ago by michealsmith ▴ 800
3
votes
2
replies
8.1k
views
Snp Filtering Based On Read-Depth In Gatk
gatk snp
updated 12.4 years ago by ▴ 300 • written 12.4 years ago by ▴ 800
0
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1
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13k
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Comment: C: Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
12.5 years ago by michealsmith ▴ 800
3
votes
8
replies
13k
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Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
updated 12.5 years ago by 7.3k • written 12.5 years ago by ▴ 800
0
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1
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13k
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Comment: C: Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
12.5 years ago by michealsmith ▴ 800
1
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0
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3.2k
views
Comment: Comment: 1000Genome Project To Cover Gc-Rich Region?
updated 4.2 years ago by 45k • written 12.6 years ago by ▴ 800
0
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0
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3.2k
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Comment: Comment: 1000Genome Project To Cover Gc-Rich Region?
updated 4.2 years ago by 45k • written 12.6 years ago by ▴ 800
4
votes
5
replies
3.2k
views
1000Genome Project To Cover Gc-Rich Region?
1000genomes
updated 4.2 years ago by 45k • written 12.6 years ago by ▴ 800
1
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1
reply
3.3k
views
Identity-By-Descent Used To Narrow Down Targets From Exome Sequencing Data
linkage
updated 12.6 years ago by 12k • written 12.6 years ago by ▴ 800
0
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1
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5.5k
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Comment: C: Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
12.6 years ago by michealsmith ▴ 800
0
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0
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5.5k
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Comment: C: Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
12.6 years ago by michealsmith ▴ 800
7
votes
5
replies
5.5k
views
Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
dbsnp
updated 12.6 years ago by ★ 1.8k • written 12.6 years ago by ▴ 800
1
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0
replies
3.7k
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Comment: C: Trio: Detecting A Large De Novo Indel
12.7 years ago by michealsmith ▴ 800
0
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1
reply
7.9k
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Comment: C: Tools For De Novo Assembly For Exome Sequencing Data
12.7 years ago by michealsmith ▴ 800
11
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7
replies
7.9k
views
Tools For De Novo Assembly For Exome Sequencing Data
assembly
updated 12.7 years ago by ▴ 960 • written 12.7 years ago by ▴ 800
2
votes
4
replies
2.2k
views
Low Productivity Of Sequencing By Hiseq2000
sequencing
12.7 years ago by michealsmith ▴ 800
0
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1
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4.3k
views
Comment: C: What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
13.0 years ago by michealsmith ▴ 800
0
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0
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4.3k
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Comment: C: What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
13.0 years ago by michealsmith ▴ 800
0
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2
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11k
views
Comment: C: Why Is Gwas Underpowered To Detect Association In Rare Variants?
13.0 years ago by michealsmith ▴ 800
25
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12
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11k
views
Why Is Gwas Underpowered To Detect Association In Rare Variants?
gwas variant
updated 13.0 years ago by 3.5k • written 13.0 years ago by ▴ 800
0
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0
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11k
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Comment: C: Why Is Gwas Underpowered To Detect Association In Rare Variants?
13.0 years ago by michealsmith ▴ 800
0
votes
0
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5.1k
views
Comment: C: Bwa Alignment: Gap Vs Soft-Clipped Sequences
13.0 years ago by michealsmith ▴ 800
0
votes
1
reply
2.0k
views
Statistical Model For Genotyping Based On Putative Structural Variants
genotyping sv
updated 13.1 years ago by ★ 1.9k • written 13.1 years ago by ▴ 800
1
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2
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3.4k
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Comment: C: Rare Variants Study Using Next-Gen Sequencing Data
13.1 years ago by michealsmith ▴ 800
6
votes
7
replies
3.4k
views
Rare Variants Study Using Next-Gen Sequencing Data
variant
updated 13.1 years ago by 12k • written 13.1 years ago by ▴ 800
10
votes
3
replies
10k
views
Minor Allele Frequency (Maf) In Dbsnp And 1000 Genome Project
maf dbsnp
updated 13.1 years ago by ▴ 690 • written 13.1 years ago by ▴ 800
0
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0
replies
10k
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Comment: C: Minor Allele Frequency (Maf) In Dbsnp And 1000 Genome Project
13.1 years ago by michealsmith ▴ 800
0
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2
replies
11k
views
Comment: C: ./ Vs "0/0" In Vcf Files
13.1 years ago by michealsmith ▴ 800
0
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0
replies
7.3k
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Comment: C: Extract Fastq From Large Bam File
13.2 years ago by michealsmith ▴ 800
2
votes
8
replies
7.3k
views
Extract Fastq From Large Bam File
fastq
13.2 years ago by michealsmith ▴ 800
0
votes
0
replies
7.3k
views
Answer: A: Extract Fastq From Large Bam File
13.2 years ago by michealsmith ▴ 800
0
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1
reply
7.3k
views
Comment: C: Extract Fastq From Large Bam File
13.2 years ago by michealsmith ▴ 800
0
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1
reply
5.0k
views
Comment: C: Vcf Format Genotyping Selection For Multisamples
13.2 years ago by michealsmith ▴ 800
0
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0
replies
7.5k
views
Answer: A: Comparison Of Two Versions Of Gatk Filtering For Exome Sequencing Data.
13.2 years ago by michealsmith ▴ 800
0
votes
0
replies
2.8k
views
Comment: C: Gatk3 Vs Dindel For Small Indel Calling
13.2 years ago by michealsmith ▴ 800
2
votes
7
replies
5.0k
views
Vcf Format Genotyping Selection For Multisamples
vcftools vcf
updated 13.2 years ago by ▴ 40 • written 13.2 years ago by ▴ 800
1
vote
2
replies
2.8k
views
Gatk3 Vs Dindel For Small Indel Calling
gatk indel
updated 13.2 years ago by 33k • written 13.2 years ago by ▴ 800
0
votes
0
replies
5.0k
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Comment: C: High-Quality Zebrafish Dbsnp Database
13.2 years ago by michealsmith ▴ 800
1
vote
2
replies
5.0k
views
High-Quality Zebrafish Dbsnp Database
dbsnp
updated 13.2 years ago by 166k • written 13.2 years ago by ▴ 800
4
votes
3
replies
7.5k
views
Comparison Of Two Versions Of Gatk Filtering For Exome Sequencing Data.
gatk
13.2 years ago by michealsmith ▴ 800
0
votes
0
replies
17k
views
Comment: C: Select Certain Column From Vcf File
13.2 years ago by michealsmith ▴ 800
91 results • Page 2 of 2
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