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Sam ♦ 2.3k
Status: New
Handle: @Sam2512
Reputation: 2320
Email: c*********@gmail.com
Joined: 8 months ago
Last seen: 9 months ago
Location: New York

Answer: A: GWAS - Relationship between Standard Error and P-value
0 Votes | 0 Replies
9 months ago
Sam
♦ 2.3k
Answer: C: Combine the polygenic scores in the individuals
2 Votes | 0 Replies
9 months ago
Sam
♦ 2.3k
Answer: A: The results of Polygenic Risk Scores(PRS)
1 Vote | 1 Reply
9 months ago
Sam
♦ 2.3k
Comment: C: The results of Polygenic Risk Scores(PRS)
1 Vote | 1 Reply
9 months ago
Sam
♦ 2.3k
Answer: A: PRSice threshold result is not as expected
1 Vote | 0 Replies
10 months ago
Sam
♦ 2.3k
Comment: C: Missing lots of SNP while clumping
0 Votes | 0 Replies
10 months ago
Sam
♦ 2.3k
Answer: A: Do we need to remove relatives for PRS calculation??
2 Votes | 0 Replies
10 months ago
Sam
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Comment: C: Plink: Understanding LD Clumping vs Pruning
0 Votes | 1 Reply
16 months ago
Sam
♦ 2.3k
Comment: C: High Kmer Content in middle of the read
0 Votes | 0 Replies
16 months ago
Sam
♦ 2.3k
Comment: C: High Kmer Content in middle of the read
0 Votes | 1 Reply
16 months ago
Sam
♦ 2.3k
High Kmer Content in middle of the read
5 Votes | 6 Replies
4.2 years ago
Sam
♦ 2.3k
• updated 16 months ago
jgarces
• 10
Comment: C: Using RNA-Seq to identify non-synonymous mutational load
1 Vote | 1 Reply
4.0 years ago
Sam
♦ 2.3k
• updated 17 months ago
RamRS
21k
Answer: A: Base file of PRSice software
0 Votes | 0 Replies
17 months ago
Sam
♦ 2.3k
Answer: A: PRSice: Imputation and clumping
1 Vote | 0 Replies
17 months ago
Sam
♦ 2.3k
Piping Markduplicates
12 Votes | 6 Replies
6.4 years ago
Sam
♦ 2.3k
• updated 2.3 years ago
rmf
• 630
Comment: C: 1000 genomes PCA for whole genome
0 Votes | 0 Replies
2.4 years ago
Sam
♦ 2.3k
Comment: C: 1000 genomes PCA for whole genome
1 Vote | 2 Replies
2.5 years ago
Sam
♦ 2.3k
Answer: A: 1000 genomes PCA for whole genome
1 Vote | 1 Reply
2.5 years ago
Sam
♦ 2.3k
Answer: A: Undrestanding BGEN files
2 Votes | 0 Replies
2.8 years ago
Sam
♦ 2.3k
Comment: C: ADMIXTURE: "Invalid chromosome code. Use integers!"
0 Votes | 0 Replies
3.0 years ago
Sam
♦ 2.3k
Comment: C: ADMIXTURE: "Invalid chromosome code. Use integers!"
0 Votes | 1 Reply
3.0 years ago
Sam
♦ 2.3k
Comment: C: ADMIXTURE: "Invalid chromosome code. Use integers!"
1 Vote | 1 Reply
3.0 years ago
Sam
♦ 2.3k
Comment: C: gene list annotation
0 Votes | 0 Replies
3.1 years ago
Sam
♦ 2.3k
Comment: C: calculate p-value for the r pairwise
0 Votes | 0 Replies
3.1 years ago
Sam
♦ 2.3k
Comment: C: calculate p-value for the r pairwise
0 Votes | 1 Reply
3.1 years ago
Sam
♦ 2.3k
Comment: C: Polygenic Risk Score PLINK
1 Vote | 0 Replies
3.2 years ago
Sam
♦ 2.3k
Comment: C: Polygenic Risk Score PLINK
0 Votes | 0 Replies
3.3 years ago
Sam
♦ 2.3k
Comment: C: RNA Sequencing Pooling design and statistic analysis
1 Vote | 0 Replies
3.4 years ago
Sam
♦ 2.3k
RNA Sequencing Pooling design and statistic analysis
5 Votes | 6 Replies
4.4 years ago
Sam
♦ 2.3k
• updated 3.4 years ago
kumarsudershan
• 0
Comment: C: filter vcf file heterozygous calls by allelic depth
0 Votes | 1 Reply
3.5 years ago
Sam
♦ 2.3k
Answer: A: R function for combining p-values
3 Votes | 0 Replies
3.5 years ago
Sam
♦ 2.3k
Comment: C: Calculating Reads And DE From BAM Files
2 Votes | 2 Replies
3.7 years ago
Sam
♦ 2.3k
Comment: C: linear regression for removing the population effects
1 Vote | 0 Replies
3.7 years ago
Sam
♦ 2.3k
Comment: C: ID Mapping code
0 Votes | 0 Replies
3.7 years ago
Sam
♦ 2.3k
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