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array jobs accessing one binary in population genetics software
population genetics software SGE
updated 5.6 years ago by 90k • written 5.6 years ago by ▴ 730
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Comment: C: illumina sequencing dual index query
5.7 years ago by prasundutta87 ▴ 730
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4.7k
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Comment: C: illumina sequencing dual index query
5.7 years ago by prasundutta87 ▴ 730
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4.7k
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Comment: C: illumina sequencing dual index query
5.7 years ago by prasundutta87 ▴ 730
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Comment: C: illumina sequencing dual index query
5.7 years ago by prasundutta87 ▴ 730
1
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10
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4.7k
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illumina sequencing dual index query
sequencing
5.7 years ago by prasundutta87 ▴ 730
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4.7k
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Comment: C: illumina sequencing dual index query
5.7 years ago by prasundutta87 ▴ 730
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Answer: A: WES allelic imbalence
5.7 years ago by prasundutta87 ▴ 730
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1
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2.2k
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soft-clipping during alignment and variant calling query
BWA-MEM GATK variant calling alignment
updated 6.0 years ago by 20 • written 6.1 years ago by ▴ 730
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1
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2.1k
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SnpEff using -onlyprotein option (meaning-Only use protein coding transcripts)
RNA-Seq SNP gene software error
updated 6.0 years ago by ★ 1.7k • written 8.7 years ago by ▴ 730
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1.3k
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candidate region selection in an XP-EHH analysis
SNP XP-EHH
updated 6.3 years ago by 20 • written 6.6 years ago by ▴ 730
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2.3k
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Answer: A: allele specific expression (ASE) reference ratio plot query
6.4 years ago by prasundutta87 ▴ 730
3
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3
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2.3k
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allele specific expression (ASE) reference ratio plot query
RNA-Seq allele-specific expression SNP
6.4 years ago by prasundutta87 ▴ 730
1
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2
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3.1k
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variant calling using reference transcriptome
RNA-Seq SNP reference transcriptome
updated 6.5 years ago by ▴ 10 • written 8.7 years ago by ▴ 730
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0
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1.3k
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finding out SNPs from SNVs and breed specific SNPs
SNP SNV
updated 6.5 years ago by 20 • written 6.6 years ago by ▴ 730
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0
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3.3k
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Answer: C: I can not run bcftools stats (help)
updated 6.6 years ago by 45k • written 6.6 years ago by ▴ 730
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2.1k
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Comment: C: outliers in XP-EHH
6.7 years ago by prasundutta87 ▴ 730
1
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2
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2.1k
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outliers in XP-EHH
population genetics outliers XP-EHH
6.7 years ago by prasundutta87 ▴ 730
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1
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5.8k
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Comment: C: Difference between Private SNPs and Singleton SNPs
6.7 years ago by prasundutta87 ▴ 730
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1
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5.8k
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Comment: C: Difference between Private SNPs and Singleton SNPs
6.7 years ago by prasundutta87 ▴ 730
7
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5
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5.8k
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Difference between Private SNPs and Singleton SNPs
SNPs GATK variant calling SNP population genetics
6.7 years ago by prasundutta87 ▴ 730
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0
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6.2k
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Correct way to report variant statistics from bcftools stats report
SNP variants statistics bcftools
6.7 years ago by prasundutta87 ▴ 730
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1
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6.9k
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Comment: C: PCAtools: everything Principal Components Analysis
6.8 years ago by prasundutta87 ▴ 730
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1
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6.9k
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Comment: A: PCAtools: everything Principal Components Analysis
6.8 years ago by prasundutta87 ▴ 730
5
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3
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1.5k
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some good practices doubts
alignment gene variant calling
updated 6.8 years ago by 20 • written 8.0 years ago by ▴ 730
1
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2
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11k
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Comment: A: HISAT2 MAPQ scoring scheme
6.9 years ago by prasundutta87 ▴ 730
2
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3.3k
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Answer: A: Paired-end flag for singleton
7.0 years ago by prasundutta87 ▴ 730
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3.9k
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Comment: C: manhattan plot with Fst values
7.0 years ago by prasundutta87 ▴ 730
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1
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3.9k
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Comment: A: manhattan plot with Fst values
7.0 years ago by prasundutta87 ▴ 730
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1
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3.1k
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Comment: C: no gene_id for tRNA in GFF3
7.0 years ago by prasundutta87 ▴ 730
1
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1
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3.1k
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Comment: C: no gene_id for tRNA in GFF3
7.0 years ago by prasundutta87 ▴ 730
0
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1
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3.1k
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Comment: C: no gene_id for tRNA in GFF3
7.0 years ago by prasundutta87 ▴ 730
0
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1
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3.1k
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Answer: C: no gene_id for tRNA in GFF3
7.0 years ago by prasundutta87 ▴ 730
4
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9
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3.1k
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no gene_id for tRNA in GFF3
annotation GFF3 GTF
7.0 years ago by prasundutta87 ▴ 730
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0
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3.1k
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Answer: A: Is HISAT2 able to output only the best alignment?
7.0 years ago by prasundutta87 ▴ 730
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2.3k
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Comment: C: allele specific expression (ASE) reference ratio plot query
7.1 years ago by prasundutta87 ▴ 730
0
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0
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1.4k
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runtime error in LDhat
genome snp LDhat population genetics
7.1 years ago by prasundutta87 ▴ 730
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2.3k
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Comment: C: Filtering results difference amongst VCF files
7.1 years ago by prasundutta87 ▴ 730
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2.3k
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Comment: C: Filtering results difference amongst VCF files
7.1 years ago by prasundutta87 ▴ 730
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1
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2.3k
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Comment: C: Filtering results difference amongst VCF files
7.1 years ago by prasundutta87 ▴ 730
2
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2.8k
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Answer: A: How to analysis mutations effects bioinformatically?
7.1 years ago by prasundutta87 ▴ 730
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6
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2.3k
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Filtering results difference amongst VCF files
SNP filtering GATK variants
7.1 years ago by prasundutta87 ▴ 730
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0
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11k
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Comment: C: GATK 4 GenomeAnalysisTK still available? (Unable to access jarfile)
7.1 years ago by prasundutta87 ▴ 730
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1
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11k
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Answer: A: GATK 4 GenomeAnalysisTK still available? (Unable to access jarfile)
7.1 years ago by prasundutta87 ▴ 730
1
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1
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4.5k
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Answer: A: best practices to use GATK with PacBio
7.1 years ago by prasundutta87 ▴ 730
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1
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3.0k
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Answer: A: Is Kallisto Sleuth pipeline suitable for all organisms?
7.2 years ago by prasundutta87 ▴ 730
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0
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1.8k
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lookup table for LDhat
population genetics ldhat software
7.2 years ago by prasundutta87 ▴ 730
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0
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18k
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Answer: A: how to count variants par sample per chromosome in a vcf file?
7.2 years ago by prasundutta87 ▴ 730
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2.3k
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Comment: C: autosomal ancestry inference
7.2 years ago by prasundutta87 ▴ 730
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5.1k
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Comment: C: PCA implementation in plink
7.2 years ago by prasundutta87 ▴ 730
261 results • Page 3 of 6
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