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1
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0
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Comment: C: Rare Variants Study Using Next-Gen Sequencing Data
11.3 years ago by michealsmith ▴ 790
3
votes
2
replies
7.6k
views
Snp Filtering Based On Read-Depth In Gatk
gatk snp
updated 11.3 years ago by ▴ 300 • written 11.3 years ago by ▴ 790
0
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1
reply
12k
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Comment: C: Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
11.4 years ago by michealsmith ▴ 790
3
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8
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12k
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Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
updated 11.4 years ago by 7.3k • written 11.4 years ago by ▴ 790
0
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1
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12k
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Comment: C: Stop-Gain Mutation Predicted As Benign By Sift/Polyphen2?
11.4 years ago by michealsmith ▴ 790
1
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0
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2.8k
views
Comment: Comment: 1000Genome Project To Cover Gc-Rich Region?
updated 3.1 years ago by 43k • written 11.4 years ago by ▴ 790
0
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0
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2.8k
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Comment: Comment: 1000Genome Project To Cover Gc-Rich Region?
updated 3.1 years ago by 43k • written 11.4 years ago by ▴ 790
4
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5
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2.8k
views
1000Genome Project To Cover Gc-Rich Region?
1000genomes
updated 3.1 years ago by 43k • written 11.4 years ago by ▴ 790
1
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1
reply
3.0k
views
Identity-By-Descent Used To Narrow Down Targets From Exome Sequencing Data
linkage
updated 11.5 years ago by 12k • written 11.5 years ago by ▴ 790
0
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1
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5.1k
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Comment: C: Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
11.5 years ago by michealsmith ▴ 790
0
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0
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5.1k
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Comment: C: Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
11.5 years ago by michealsmith ▴ 790
7
votes
5
replies
5.1k
views
Snps Present In Dbsnp But Absent In 1000Genome And Esp Database
dbsnp
updated 11.5 years ago by ★ 1.8k • written 11.5 years ago by ▴ 790
1
vote
0
replies
3.2k
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Comment: C: Trio: Detecting A Large De Novo Indel
11.5 years ago by michealsmith ▴ 790
0
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1
reply
7.2k
views
Comment: C: Tools For De Novo Assembly For Exome Sequencing Data
11.5 years ago by michealsmith ▴ 790
11
votes
7
replies
7.2k
views
Tools For De Novo Assembly For Exome Sequencing Data
assembly
updated 11.5 years ago by ▴ 940 • written 11.5 years ago by ▴ 790
2
votes
4
replies
1.9k
views
Low Productivity Of Sequencing By Hiseq2000
sequencing
11.6 years ago by michealsmith ▴ 790
0
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1
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3.8k
views
Comment: C: What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
11.8 years ago by michealsmith ▴ 790
0
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0
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3.8k
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Comment: C: What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
11.9 years ago by michealsmith ▴ 790
0
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2
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9.3k
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Comment: C: Why Is Gwas Underpowered To Detect Association In Rare Variants?
11.9 years ago by michealsmith ▴ 790
21
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12
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9.3k
views
Why Is Gwas Underpowered To Detect Association In Rare Variants?
gwas variant
updated 11.9 years ago by 3.5k • written 11.9 years ago by ▴ 790
0
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0
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9.3k
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Comment: C: Why Is Gwas Underpowered To Detect Association In Rare Variants?
11.9 years ago by michealsmith ▴ 790
0
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0
replies
4.8k
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Comment: C: Bwa Alignment: Gap Vs Soft-Clipped Sequences
11.9 years ago by michealsmith ▴ 790
0
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1
reply
1.8k
views
Statistical Model For Genotyping Based On Putative Structural Variants
genotyping sv
updated 11.9 years ago by ★ 1.8k • written 11.9 years ago by ▴ 790
1
vote
2
replies
2.9k
views
Comment: C: Rare Variants Study Using Next-Gen Sequencing Data
12.0 years ago by michealsmith ▴ 790
6
votes
7
replies
2.9k
views
Rare Variants Study Using Next-Gen Sequencing Data
variant
updated 12.0 years ago by 12k • written 12.0 years ago by ▴ 790
10
votes
3
replies
9.6k
views
Minor Allele Frequency (Maf) In Dbsnp And 1000 Genome Project
maf dbsnp
updated 12.0 years ago by ▴ 690 • written 12.0 years ago by ▴ 790
0
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0
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9.6k
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Comment: C: Minor Allele Frequency (Maf) In Dbsnp And 1000 Genome Project
12.0 years ago by michealsmith ▴ 790
0
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2
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10k
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Comment: C: ./ Vs "0/0" In Vcf Files
12.0 years ago by michealsmith ▴ 790
0
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0
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6.8k
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Comment: C: Extract Fastq From Large Bam File
12.0 years ago by michealsmith ▴ 790
2
votes
8
replies
6.8k
views
Extract Fastq From Large Bam File
fastq
12.0 years ago by michealsmith ▴ 790
0
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0
replies
6.8k
views
Answer: A: Extract Fastq From Large Bam File
12.0 years ago by michealsmith ▴ 790
0
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1
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6.8k
views
Comment: C: Extract Fastq From Large Bam File
12.0 years ago by michealsmith ▴ 790
0
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1
reply
4.6k
views
Comment: C: Vcf Format Genotyping Selection For Multisamples
12.0 years ago by michealsmith ▴ 790
0
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0
replies
7.2k
views
Answer: A: Comparison Of Two Versions Of Gatk Filtering For Exome Sequencing Data.
12.0 years ago by michealsmith ▴ 790
0
votes
0
replies
2.6k
views
Comment: C: Gatk3 Vs Dindel For Small Indel Calling
12.0 years ago by michealsmith ▴ 790
2
votes
7
replies
4.6k
views
Vcf Format Genotyping Selection For Multisamples
vcftools vcf
updated 12.0 years ago by ▴ 40 • written 12.0 years ago by ▴ 790
1
vote
2
replies
2.6k
views
Gatk3 Vs Dindel For Small Indel Calling
gatk indel
updated 12.0 years ago by 33k • written 12.0 years ago by ▴ 790
0
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0
replies
4.7k
views
Comment: C: High-Quality Zebrafish Dbsnp Database
12.1 years ago by michealsmith ▴ 790
1
vote
2
replies
4.7k
views
High-Quality Zebrafish Dbsnp Database
dbsnp
updated 12.1 years ago by 161k • written 12.1 years ago by ▴ 790
4
votes
3
replies
7.2k
views
Comparison Of Two Versions Of Gatk Filtering For Exome Sequencing Data.
gatk
12.1 years ago by michealsmith ▴ 790
0
votes
0
replies
16k
views
Comment: C: Select Certain Column From Vcf File
12.1 years ago by michealsmith ▴ 790
91 results • Page 2 of 2
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