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Answer: A: Mismatch between base and target genotypes causing a "no variants remained" erro
4.1 years ago by Sam ★ 4.7k
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589
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Answer: A: GWAS data integration
4.1 years ago by Sam ★ 4.7k
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Answer: A: Questions about Polygenic Risk Score (PRS) and PRSice-2
4.2 years ago by Sam ★ 4.7k
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Answer: A: Hwo to do quality control steps on UKBiobank data?
4.2 years ago by Sam ★ 4.7k
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Answer: A: Do you always need to clump polygenic risk scores?
4.2 years ago by Sam ★ 4.7k
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2.7k
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Answer: A: How to load 1000 genome vcf and tbi file into R
4.2 years ago by Sam ★ 4.7k
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Answer: A: Effect Allele Frequency in base summary statistics for PRSs calculation
4.2 years ago by Sam ★ 4.7k
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Answer: A: Can tophat/cufflinks output vary on different runs?
updated 4.3 years ago by 43k • written 9.9 years ago by ★ 4.7k
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Answer: A: Correlation of PRS obtained by plink and PRSice
4.4 years ago by Sam ★ 4.7k
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2.0k
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Answer: A: Which software should be used to get SNPs different from reference but same in a
updated 4.4 years ago by 43k • written 10.0 years ago by ★ 4.7k
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1.8k
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Answer: A: How to estimate SNP-based heritability?
4.4 years ago by Sam ★ 4.7k
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Answer: C: Valine to Isoleucine mutation
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 4.7k
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2.2k
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Answer: C: What variant callers are faster than samtools?
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 4.7k
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Answer: A: Batch replcement of fasta header
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 4.7k
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1
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7.8k
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Answer: A: GenomeStudio genotype format to VCF?
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 4.7k
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Answer: A: GATK 3.8 > GATK 4 best way to step up
4.4 years ago by Sam ★ 4.7k
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2.4k
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Answer: A: Applying polygenic scores to data
4.5 years ago by Sam ★ 4.7k
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3.6k
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Answer: A: variance stabilized or log transformed data for DE analysis
updated 4.5 years ago by 43k • written 8.6 years ago by ★ 4.7k
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0
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3.9k
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Answer: A: edegR, export TMM normalized method
updated 4.5 years ago by 43k • written 8.6 years ago by ★ 4.7k
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1
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4.4k
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Answer: C: What suggestive line at manhattan plot usually stands for?
4.5 years ago by Sam ★ 4.7k
4
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1
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3.3k
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Answer: Answer: Concordance analysis using statistics/graphs/figures
updated 16 months ago by 43k • written 8.9 years ago by ★ 4.7k
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1
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999
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Answer: A: Linear regression on subsets of data corresponding to two factor combination
4.6 years ago by Sam ★ 4.7k
3
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1
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4.6k
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Answer: A: Open Source Variant Caller comparable to GATK Haplotype Caller?
updated 4.6 years ago by 43k • written 9.6 years ago by ★ 4.7k
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Answer: A: New to RNA-Seq: Reads assembled...now what? Non-sequenced organism. So lost!!
updated 4.6 years ago by 43k • written 9.9 years ago by ★ 4.7k
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Answer: A: Disease risk calculation
4.7 years ago by Sam ★ 4.7k
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1
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1.4k
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Answer: C: install tophat on windows
4.7 years ago by Sam ★ 4.7k
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1
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874
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Answer: A: Meta analysis on 2 genotyping data set
4.8 years ago by Sam ★ 4.7k
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964
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Answer: A: Estimate the genomic relationship between Discovery and Target sample in PRS
4.8 years ago by Sam ★ 4.7k
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2.3k
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Answer: A: WGCNA Different Module Results
4.9 years ago by Sam ★ 4.7k
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4.9k
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Answer: C: polygenic risk score
4.9 years ago by Sam ★ 4.7k
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1
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1.9k
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Answer: A: Adjusting binary phenotype (case/ctrl) for Polygenic Risk Score (PRS)
4.9 years ago by Sam ★ 4.7k
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2
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1.6k
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Answer: A: Match column row wise and do calculations
4.9 years ago by Sam ★ 4.7k
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1
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3.4k
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Answer: A: GWAS - Relationship between Standard Error and P-value
5.0 years ago by Sam ★ 4.7k
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1.5k
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Answer: C: Combine the polygenic scores in the individuals
5.0 years ago by Sam ★ 4.7k
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1
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2.0k
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Answer: A: The results of Polygenic Risk Scores(PRS)
5.0 years ago by Sam ★ 4.7k
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1.9k
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Answer: A: PRSice PRS calculation warning Mismatched SNPs. Is it due to using multi-covaria
5.1 years ago by Sam ★ 4.7k
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0
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1.2k
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Answer: A: PRSice threshold result is not as expected
5.1 years ago by Sam ★ 4.7k
2
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2
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3.1k
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Answer: A: The effect of sample size and relatedness in target sample in polygenic risk sco
5.1 years ago by Sam ★ 4.7k
3
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1.5k
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Answer: A: Do we need to remove relatives for PRS calculation??
5.1 years ago by Sam ★ 4.7k
2
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3.2k
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Answer: A: How to calculate Polygenic Risk Score from Summary Results with Z-Score only
5.3 years ago by Sam ★ 4.7k
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1.1k
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Answer: A: Estimating SNP heritability for related individuals from a SNP array
5.3 years ago by Sam ★ 4.7k
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2.6k
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Answer: A: Base file of PRSice software
5.7 years ago by Sam ★ 4.7k
2
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3.2k
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Answer: A: PRSice: Imputation and clumping
5.7 years ago by Sam ★ 4.7k
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2.0k
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Answer: A: GWAS: How to estimate probability of SNP association being result of one specifi
6.7 years ago by Sam ★ 4.7k
2
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1
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4.9k
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Answer: A: 1000 genomes PCA for whole genome
6.7 years ago by Sam ★ 4.7k
2
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0
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6.9k
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Answer: A: Undrestanding BGEN files
7.0 years ago by Sam ★ 4.7k
6
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0
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6.9k
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Answer: A: R function for combining p-values
7.7 years ago by Sam ★ 4.7k
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0
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2.9k
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Answer: A: How to see bim file in genomics?
8.0 years ago by Sam ★ 4.7k
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1
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2.0k
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Answer: A: R for loop
8.2 years ago by Sam ★ 4.7k
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0
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878
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Answer: A: In Case of Transcriptomic data
8.2 years ago by Sam ★ 4.7k
201 results • Page 3 of 5
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