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Comment: C: illumina sequencing dual index query
4.2 years ago by prasundutta87 ▴ 660
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3.1k
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Comment: C: illumina sequencing dual index query
4.2 years ago by prasundutta87 ▴ 660
0
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1
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3.1k
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Comment: C: illumina sequencing dual index query
4.2 years ago by prasundutta87 ▴ 660
0
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0
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3.1k
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Comment: C: illumina sequencing dual index query
4.2 years ago by prasundutta87 ▴ 660
1
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10
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3.1k
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illumina sequencing dual index query
sequencing
4.2 years ago by prasundutta87 ▴ 660
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1
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3.1k
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Comment: C: illumina sequencing dual index query
4.2 years ago by prasundutta87 ▴ 660
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751
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Answer: A: WES allelic imbalence
4.2 years ago by prasundutta87 ▴ 660
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1
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1.8k
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soft-clipping during alignment and variant calling query
BWA-MEM GATK variant calling alignment
updated 4.5 years ago by 20 • written 4.5 years ago by ▴ 660
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1
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1.7k
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SnpEff using -onlyprotein option (meaning-Only use protein coding transcripts)
RNA-Seq SNP gene software error
updated 4.5 years ago by ★ 1.5k • written 7.2 years ago by ▴ 660
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0
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1.0k
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candidate region selection in an XP-EHH analysis
SNP XP-EHH
updated 4.7 years ago by 20 • written 5.1 years ago by ▴ 660
3
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3
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1.6k
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allele specific expression (ASE) reference ratio plot query
RNA-Seq allele-specific expression SNP
4.8 years ago by prasundutta87 ▴ 660
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0
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1.6k
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Answer: A: allele specific expression (ASE) reference ratio plot query
4.8 years ago by prasundutta87 ▴ 660
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2
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2.7k
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variant calling using reference transcriptome
RNA-Seq SNP reference transcriptome
updated 4.9 years ago by ▴ 10 • written 7.1 years ago by ▴ 660
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0
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1.0k
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finding out SNPs from SNVs and breed specific SNPs
SNP SNV
updated 4.9 years ago by 20 • written 5.0 years ago by ▴ 660
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0
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2.4k
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Answer: C: I can not run bcftools stats (help)
updated 5.1 years ago by 43k • written 5.1 years ago by ▴ 660
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0
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1.5k
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Comment: C: outliers in XP-EHH
5.1 years ago by prasundutta87 ▴ 660
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2
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1.5k
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outliers in XP-EHH
population genetics outliers XP-EHH
5.1 years ago by prasundutta87 ▴ 660
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1
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4.8k
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Comment: C: Difference between Private SNPs and Singleton SNPs
5.2 years ago by prasundutta87 ▴ 660
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1
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4.8k
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Comment: C: Difference between Private SNPs and Singleton SNPs
5.2 years ago by prasundutta87 ▴ 660
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5
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4.8k
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Difference between Private SNPs and Singleton SNPs
SNPs GATK variant calling SNP population genetics
5.2 years ago by prasundutta87 ▴ 660
0
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0
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5.6k
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Correct way to report variant statistics from bcftools stats report
SNP variants statistics bcftools
5.2 years ago by prasundutta87 ▴ 660
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1
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5.0k
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Comment: C: PCAtools: everything Principal Components Analysis
5.2 years ago by prasundutta87 ▴ 660
1
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1
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5.0k
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Comment: A: PCAtools: everything Principal Components Analysis
5.2 years ago by prasundutta87 ▴ 660
5
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3
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1.1k
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some good practices doubts
alignment gene variant calling
updated 5.3 years ago by 20 • written 6.4 years ago by ▴ 660
1
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2
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8.8k
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Comment: A: HISAT2 MAPQ scoring scheme
5.3 years ago by prasundutta87 ▴ 660
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0
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2.4k
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Answer: A: Paired-end flag for singleton
5.4 years ago by prasundutta87 ▴ 660
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0
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3.3k
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Comment: C: manhattan plot with Fst values
5.4 years ago by prasundutta87 ▴ 660
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1
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3.3k
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Comment: A: manhattan plot with Fst values
5.4 years ago by prasundutta87 ▴ 660
0
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1
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2.2k
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Comment: C: no gene_id for tRNA in GFF3
5.5 years ago by prasundutta87 ▴ 660
1
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1
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2.2k
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Comment: C: no gene_id for tRNA in GFF3
5.5 years ago by prasundutta87 ▴ 660
0
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1
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2.2k
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Comment: C: no gene_id for tRNA in GFF3
5.5 years ago by prasundutta87 ▴ 660
0
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1
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2.2k
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Answer: C: no gene_id for tRNA in GFF3
5.5 years ago by prasundutta87 ▴ 660
4
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9
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2.2k
views
no gene_id for tRNA in GFF3
annotation GFF3 GTF
5.5 years ago by prasundutta87 ▴ 660
0
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0
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2.5k
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Answer: A: Is HISAT2 able to output only the best alignment?
5.5 years ago by prasundutta87 ▴ 660
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1.6k
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Comment: C: allele specific expression (ASE) reference ratio plot query
5.5 years ago by prasundutta87 ▴ 660
0
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0
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1.1k
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runtime error in LDhat
genome snp LDhat population genetics
5.5 years ago by prasundutta87 ▴ 660
0
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0
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1.7k
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Comment: C: Filtering results difference amongst VCF files
5.6 years ago by prasundutta87 ▴ 660
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1.7k
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Comment: C: Filtering results difference amongst VCF files
5.6 years ago by prasundutta87 ▴ 660
0
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1
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1.7k
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Comment: C: Filtering results difference amongst VCF files
5.6 years ago by prasundutta87 ▴ 660
2
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0
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1.9k
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Answer: A: How to analysis mutations effects bioinformatically?
5.6 years ago by prasundutta87 ▴ 660
0
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6
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1.7k
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Filtering results difference amongst VCF files
SNP filtering GATK variants
5.6 years ago by prasundutta87 ▴ 660
0
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0
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8.7k
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Comment: C: GATK 4 GenomeAnalysisTK still available? (Unable to access jarfile)
5.6 years ago by prasundutta87 ▴ 660
0
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1
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8.7k
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Answer: A: GATK 4 GenomeAnalysisTK still available? (Unable to access jarfile)
5.6 years ago by prasundutta87 ▴ 660
1
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1
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3.9k
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Answer: A: best practices to use GATK with PacBio
5.6 years ago by prasundutta87 ▴ 660
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1
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2.4k
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Answer: A: Is Kallisto Sleuth pipeline suitable for all organisms?
5.6 years ago by prasundutta87 ▴ 660
0
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0
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1.5k
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lookup table for LDhat
population genetics ldhat software
5.6 years ago by prasundutta87 ▴ 660
0
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0
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14k
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Answer: A: how to count variants par sample per chromosome in a vcf file?
5.6 years ago by prasundutta87 ▴ 660
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0
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1.8k
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Comment: C: autosomal ancestry inference
5.7 years ago by prasundutta87 ▴ 660
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4.2k
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Comment: C: PCA implementation in plink
5.7 years ago by prasundutta87 ▴ 660
2
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2
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4.2k
views
PCA implementation in plink
Plink PCA population
updated 5.7 years ago by 10k • written 5.7 years ago by ▴ 660
260 results • Page 3 of 6
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