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9.3k
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Answer: A: How can I filter a vcf file by DP and GQ using the R package VariantAnnotation?
10.6 years ago by NB ▴ 960
0
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0
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3.9k
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Comment: C: how to generate setID file?
10.6 years ago by NB ▴ 960
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0
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9.0k
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Comment: C: Where can I download NCI 60 data?
10.6 years ago by NB ▴ 960
0
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0
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2.4k
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Comment: Comment: Getting colors when displaying .bed files in locuszoom1.3
updated 3.6 years ago by 45k • written 10.7 years ago by ▴ 960
0
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1
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2.3k
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Tools/Softwares to find proxies for Indels
indels proxies
updated 3.5 years ago by 45k • written 10.8 years ago by ▴ 960
2
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1
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2.4k
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NGSrich target enrichment: software error
software error NGSrich
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 960
0
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1
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8.6k
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Comment: C: Plink allele scoring output
10.8 years ago by NB ▴ 960
0
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1
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8.6k
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Comment: C: Plink allele scoring output
10.8 years ago by NB ▴ 960
9
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5
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8.6k
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Plink allele scoring output
plink allele-scoring
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 960
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0
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3.7k
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conditional analysis and gene-wide analysis
conditional analysis gene-wide analysis interpret
updated 10.9 years ago by 20 • written 11.0 years ago by ▴ 960
2
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0
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3.4k
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Answer: A: where to get the gene annotations for the latest build 37 - for plotting regiona
10.9 years ago by NB ▴ 960
0
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0
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8.0k
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Answer: Answer: How to draw venn diagram for two CNV lists?
updated 3.5 years ago by 45k • written 10.9 years ago by ▴ 960
0
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0
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20k
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Comment: C: Pros and cons of Illumina HiSeq and Next Seq
10.9 years ago by NB ▴ 960
0
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1
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20k
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Comment: C: Pros and cons of Illumina HiSeq and Next Seq
10.9 years ago by NB ▴ 960
5
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6
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20k
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Pros and cons of Illumina HiSeq and Next Seq
hi-seq illumina next-seq
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 960
1
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2
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6.8k
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Answer: Answer: samtools-1.1 rmdup error
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 960
0
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0
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3.6k
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Comment: C: bam file readgroup to include several individuals
11.0 years ago by NB ▴ 960
0
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0
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2.7k
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Comment: C: plotting pvalues from 2 data sets
11.0 years ago by NB ▴ 960
0
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1
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2.7k
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Comment: C: plotting pvalues from 2 data sets
11.0 years ago by NB ▴ 960
2
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4
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2.7k
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plotting pvalues from 2 data sets
pvalues plots
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 960
0
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0
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12k
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Comment: C: Create Interval List for Picard CollectRNASeqmetrics
11.0 years ago by NB ▴ 960
1
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0
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4.0k
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Comment: C: Memory Allocation for VarScan
11.0 years ago by NB ▴ 960
2
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1
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5.6k
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Comment: C: CNV frequencies and MAF
11.0 years ago by NB ▴ 960
1
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1
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5.3k
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Comment: Comment: How to find genes that are involved in particular pathway ?
updated 3.8 years ago by 45k • written 11.0 years ago by ▴ 960
0
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4
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2.2k
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follow-up on a significant variant/Gene
protein follow-up SNP
updated 3.8 years ago by 45k • written 11.1 years ago by ▴ 960
0
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1
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2.2k
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Comment: C: follow-up on a significant variant/Gene
11.1 years ago by NB ▴ 960
0
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0
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2.3k
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Answer: Answer: Minor allele frequency and damaging prediction
updated 3.8 years ago by 45k • written 11.1 years ago by ▴ 960
0
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0
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4.1k
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Comment: Comment: extract SNPs from compressed PLINK files
updated 3.8 years ago by 45k • written 11.1 years ago by ▴ 960
0
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2
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4.1k
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extract SNPs from compressed PLINK files
PLINK
updated 3.8 years ago by 45k • written 11.1 years ago by ▴ 960
5
votes
5
replies
8.2k
views
Convert .Pre Files To .Ped And .Map Files For Plink
plink
updated 11.2 years ago by ▴ 40 • written 13.5 years ago by ▴ 960
0
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0
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7.1k
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Comment: C: Low Coverage Depth On Exome Sequencing
11.6 years ago by NB ▴ 960
5
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3
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7.1k
views
Low Coverage Depth On Exome Sequencing
exome-sequencing coverage
updated 11.6 years ago by ★ 1.1k • written 11.6 years ago by ▴ 960
5
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6
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5.3k
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How Can I Annotate Cnvs
cnv
updated 11.6 years ago by ▴ 90 • written 12.6 years ago by ▴ 960
2
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0
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5.4k
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Comment: C: Tools For Predicting Functional Effects Of Snps?
12.1 years ago by NB ▴ 960
0
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1
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2.3k
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Comment: C: Is There A Tool That Would Directly Encode Minor Alllele Freq In The Info Column
12.2 years ago by NB ▴ 960
0
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0
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2.7k
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Comment: C: How Can I Overlay My Snp Variants With Various Databases
12.3 years ago by NB ▴ 960
0
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2
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2.7k
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How Can I Overlay My Snp Variants With Various Databases
1000genomes hapmap dbsnp
updated 12.3 years ago by ▴ 120 • written 12.5 years ago by ▴ 960
0
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0
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2.2k
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Comment: C: Why Is The Snp Info Missing From Dbsnp ?
12.4 years ago by NB ▴ 960
4
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5
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2.2k
views
Why Is The Snp Info Missing From Dbsnp ?
snp dbsnp
updated 12.4 years ago by 14k • written 12.4 years ago by ▴ 960
2
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1
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2.2k
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Comment: C: Why Is The Snp Info Missing From Dbsnp ?
12.4 years ago by NB ▴ 960
0
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1
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7.5k
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Comment: C: Automated Literature Search For List Of Genes
12.4 years ago by NB ▴ 960
1
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2
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10k
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Answer: A: Picard Markduplicates Error: Requested Array Size Exceeds Vm Limit
12.5 years ago by NB ▴ 960
0
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0
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5.3k
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Comment: C: How Can I Annotate Cnvs
12.6 years ago by NB ▴ 960
1
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0
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8.5k
views
Comment: C: How To Revert Allele Data To Atgc With Plink After Recoding To 12 Format
12.6 years ago by NB ▴ 960
0
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1
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8.5k
views
Comment: C: How To Revert Allele Data To Atgc With Plink After Recoding To 12 Format
updated 12.6 years ago by 28k • written 12.6 years ago by ▴ 960
5
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1
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8.5k
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Answer: A: How To Revert Allele Data To Atgc With Plink After Recoding To 12 Format
12.6 years ago by NB ▴ 960
0
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0
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7.9k
views
Comment: C: How To Create Cluster Files For Plink When Performing A Stratified Analysis On T
12.6 years ago by NB ▴ 960
1
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5
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7.9k
views
How To Create Cluster Files For Plink When Performing A Stratified Analysis On Three Different Population Datasets
deleted-post
updated 12.6 years ago by 103k • written 12.6 years ago by ▴ 960
0
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1
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7.9k
views
Comment: C: How To Create Cluster Files For Plink When Performing A Stratified Analysis On T
12.6 years ago by NB ▴ 960
3
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1
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2.0k
views
Where To Obtain The Allele Frequency Information Of The 200 Danish Exomes?
hg19
updated 12.7 years ago by 103k • written 12.7 years ago by ▴ 960
210 results • Page 4 of 5
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