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Comment: Comment: 1000 Genome Project and ESP for indel or frameshift
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
0
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1
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2.6k
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Comment: Comment: 1000 Genome Project and ESP for indel or frameshift
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
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0
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79k
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Comment: Comment: What Are Phased And Unphased Genotypes?
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
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0
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4.2k
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Comment: Comment: gene function in refgene when using annovar
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
1
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2
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4.2k
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gene function in refgene when using annovar
annovar
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
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1.7k
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Comment: C: Dot mark in 1000 genome project
10.0 years ago by 897598644 ▴ 100
1
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2
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1.7k
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Dot mark in 1000 genome project
annovar
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
0
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0
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956
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how many bases in the number of inter-individual difference on average ?
next-gen-sequencing
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
0
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1
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1.8k
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Comment: C: base quality in the result of mpileup
10.0 years ago by 897598644 ▴ 100
3
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3
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1.8k
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base quality in the result of mpileup
next-gen-sequencing
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 100
0
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1
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2.5k
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Comment: Comment: How to get coverage ratio?
updated 2.8 years ago by 44k • written 10.1 years ago by ▴ 100
2
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4
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2.5k
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How to get coverage ratio?
sequence next-gen-sequencing
updated 2.8 years ago by 44k • written 10.1 years ago by ▴ 100
0
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1
reply
1.5k
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base and genotype at the same position
SNP next-gen-sequencing
updated 2.9 years ago by 44k • written 10.1 years ago by ▴ 100
0
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1
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3.2k
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Comment: C: variant call format
10.1 years ago by 897598644 ▴ 100
4
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14
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3.2k
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variant call format
next-gen-sequencing
updated 2.9 years ago by 44k • written 10.1 years ago by ▴ 100
0
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2
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3.2k
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Comment: Comment: variant call format
10.1 years ago by 897598644 ▴ 100
0
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1
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3.2k
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Comment: C: variant call format
10.1 years ago by 897598644 ▴ 100
0
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1
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3.2k
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Comment: Comment: variant call format
updated 2.9 years ago by 44k • written 10.1 years ago by ▴ 100
0
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1
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3.2k
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Comment: Comment: variant call format
updated 2.9 years ago by 44k • written 10.1 years ago by ▴ 100
0
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0
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3.2k
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Comment: C: variant call format
10.1 years ago by 897598644 ▴ 100
1
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1
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3.1k
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MAX_FILE_HANDLES_FOR_READ_ENDS_MAP=8000 in picard use
next-gen-sequencing
updated 3.0 years ago by 44k • written 10.1 years ago by ▴ 100
0
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1
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2.4k
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Comment: Comment: where are parameters of SNPQ(snp quality) and TD(total read depth) defined when
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
1
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3
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2.4k
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where are parameters of SNPQ(snp quality) and TD(total read depth) defined when calling variants using SAMTOOLS and GATK?
next-gen sequencing alignment
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
0
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1
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3.3k
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Comment: Comment: how to filter at the information of DP(read depth at this position for this samp
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
0
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1
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3.3k
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Comment: Comment: how to filter at the information of DP(read depth at this position for this samp
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
2
votes
6
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3.3k
views
how to filter at the information of DP(read depth at this position for this sample (Integer))
next-gen sequencing
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
6
votes
1
reply
3.4k
views
How to find structural variants
next-gen sequencing genome
updated 3.7 years ago by 44k • written 10.2 years ago by ▴ 100
0
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1
reply
7.8k
views
Comment: Comment: Annovar Annotation With 1000G
updated 2.9 years ago by 44k • written 10.2 years ago by ▴ 100
0
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1
reply
11k
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Comment: C: how to identify a sequencing sample's gender
10.3 years ago by 897598644 ▴ 100
0
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1
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11k
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Comment: Comment: how to identify a sequencing sample's gender
updated 3.0 years ago by 44k • written 10.3 years ago by ▴ 100
11
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17
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11k
views
9 follow
how to identify a sequencing sample's gender
genome next-gen-sequencing
updated 3.0 years ago by 44k • written 10.3 years ago by ▴ 100
0
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1
reply
11k
views
Comment: C: how to identify a sequencing sample's gender
10.3 years ago by 897598644 ▴ 100
0
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0
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3.9k
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Comment: Comment: How to find de novo mutation in trio sequencing data in perl or python script?
updated 3.0 years ago by 44k • written 10.3 years ago by ▴ 100
0
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0
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4.1k
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Comment: Comment: Variants with extreme strand bias in HiSeq2500 data
updated 3.0 years ago by 44k • written 10.3 years ago by ▴ 100
0
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0
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9.4k
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Comment: Comment: Identifying De Novo Variants In Trio Data
updated 3.0 years ago by 44k • written 10.3 years ago by ▴ 100
1
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1
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3.9k
views
Comment: Comment: How to find de novo mutation in trio sequencing data in perl or python script?
updated 2.9 years ago by 44k • written 10.3 years ago by ▴ 100
7
votes
4
replies
3.9k
views
How to find de novo mutation in trio sequencing data in perl or python script?
next-gen sequencing gene snp
updated 2.9 years ago by 44k • written 10.3 years ago by ▴ 100
0
votes
1
reply
4.5k
views
Comment: C: phasing de novo mutations
10.3 years ago by 897598644 ▴ 100
88 results • Page 2 of 2
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