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Comment:
Comment: websites about finding genes assiociated with rare-disease which is unreported b
updated 19 months ago by
Ram
43k • written 8.8 years ago by
NB
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1
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20k
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Comment:
C: Calculate z-scores from GWAS summary stats
9.1 years ago by
NB
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4.6k
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Comment:
Comment: eQTL analysis: Genotyping data, microarray expression data
updated 2.1 years ago by
Ram
43k • written 9.1 years ago by
NB
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2.1k
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Comment:
C: Single nucleotide Polymorphism (SNP)
9.1 years ago by
NB
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3.4k
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Comment:
C: Pathway classification of genes
9.1 years ago by
NB
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3.4k
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Comment:
C: how to generate setID file?
9.2 years ago by
NB
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7.7k
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Comment:
C: Where can I download NCI 60 data?
9.2 years ago by
NB
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2.1k
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Comment:
Comment: Getting colors when displaying .bed files in locuszoom1.3
updated 2.2 years ago by
Ram
43k • written 9.2 years ago by
NB
▴ 960
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1
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7.2k
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Comment:
C: Plink allele scoring output
9.3 years ago by
NB
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1
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7.2k
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Comment:
C: Plink allele scoring output
9.3 years ago by
NB
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18k
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Comment:
C: Pros and cons of Illumina HiSeq and Next Seq
9.5 years ago by
NB
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1
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18k
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Comment:
C: Pros and cons of Illumina HiSeq and Next Seq
9.5 years ago by
NB
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3.0k
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Comment:
C: bam file readgroup to include several individuals
9.5 years ago by
NB
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2.3k
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Comment:
C: plotting pvalues from 2 data sets
9.5 years ago by
NB
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1
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2.3k
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Comment:
C: plotting pvalues from 2 data sets
9.5 years ago by
NB
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11k
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Comment:
C: Create Interval List for Picard CollectRNASeqmetrics
9.5 years ago by
NB
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3.4k
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Comment:
C: Memory Allocation for VarScan
9.5 years ago by
NB
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1
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4.8k
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Comment:
C: CNV frequencies and MAF
9.5 years ago by
NB
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1
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4.5k
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Comment:
Comment: How to find genes that are involved in particular pathway ?
updated 2.3 years ago by
Ram
43k • written 9.6 years ago by
NB
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1
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1.9k
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Comment:
C: follow-up on a significant variant/Gene
9.6 years ago by
NB
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3.7k
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Comment:
Comment: extract SNPs from compressed PLINK files
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
NB
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6.3k
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Comment:
C: Low Coverage Depth On Exome Sequencing
10.1 years ago by
NB
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4.5k
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Comment:
C: Tools For Predicting Functional Effects Of Snps?
10.7 years ago by
NB
▴ 960
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1
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1.9k
views
Comment:
C: Is There A Tool That Would Directly Encode Minor Alllele Freq In The Info Column
10.8 years ago by
NB
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2.3k
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Comment:
C: How Can I Overlay My Snp Variants With Various Databases
10.9 years ago by
NB
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1.7k
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Comment:
C: Why Is The Snp Info Missing From Dbsnp ?
10.9 years ago by
NB
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2
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1
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1.7k
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Comment:
C: Why Is The Snp Info Missing From Dbsnp ?
10.9 years ago by
NB
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1
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6.1k
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Comment:
C: Automated Literature Search For List Of Genes
10.9 years ago by
NB
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4.5k
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Comment:
C: How Can I Annotate Cnvs
11.1 years ago by
NB
▴ 960
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7.7k
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Comment:
C: How To Revert Allele Data To Atgc With Plink After Recoding To 12 Format
11.2 years ago by
NB
▴ 960
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1
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7.7k
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Comment:
C: How To Revert Allele Data To Atgc With Plink After Recoding To 12 Format
updated 11.2 years ago by
Giovanni M Dall'Olio
28k • written 11.2 years ago by
NB
▴ 960
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7.4k
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Comment:
C: How To Create Cluster Files For Plink When Performing A Stratified Analysis On T
11.2 years ago by
NB
▴ 960
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1
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7.4k
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Comment:
C: How To Create Cluster Files For Plink When Performing A Stratified Analysis On T
11.2 years ago by
NB
▴ 960
0
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2.2k
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Comment:
C: Matching The Entries And Printing Data
11.6 years ago by
NB
▴ 960
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1
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2.2k
views
Comment:
C: Matching The Entries And Printing Data
11.6 years ago by
NB
▴ 960
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votes
1
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11k
views
Comment:
C: Cnvnator Output File
11.9 years ago by
NB
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1
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7.5k
views
Comment:
C: Convert .Pre Files To .Ped And .Map Files For Plink
12.0 years ago by
NB
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votes
1
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10k
views
Comment:
C: Whole Genome Analysis Pipeline (Illumina)
12.1 years ago by
NB
▴ 960
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