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Answer: Answer: How to parse the output file of snpEFF
20 months ago by prasundutta87 ▴ 660
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1.4k
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Answer: Answer: EPIC array data - How to find the total number of genes in the array?
2.5 years ago by prasundutta87 ▴ 660
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1.9k
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Answer: Answer: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
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573
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Answer: Answer: calculation of gene coverage
2.5 years ago by prasundutta87 ▴ 660
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2.1k
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Answer: Answer: Extract CDS from maker gff
2.8 years ago by prasundutta87 ▴ 660
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1.5k
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Answer: Answer: Given my background, what are my chances of being accepted into a PhD program at
2.9 years ago by prasundutta87 ▴ 660
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819
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Answer: Answer: How can a mapping be performed without alignment?
2.9 years ago by prasundutta87 ▴ 660
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911
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Answer: Answer: PCA plot making
3.1 years ago by prasundutta87 ▴ 660
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1.7k
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Answer: Answer: remove unmapped reads on a specific chromosome only
3.1 years ago by prasundutta87 ▴ 660
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2.1k
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Answer: A: Read VEP output from command line in R
3.1 years ago by prasundutta87 ▴ 660
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975
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Answer: A: Human Exome Variant Reference
3.2 years ago by prasundutta87 ▴ 660
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3.2k
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Answer: A: Determine the sex of a sample from a .vcf
3.2 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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1.6k
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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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2.4k
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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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2.4k
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Answer: A: Paired-end flag for singleton
5.4 years ago by prasundutta87 ▴ 660
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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
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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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1.9k
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Answer: A: How to analysis mutations effects bioinformatically?
5.6 years ago by prasundutta87 ▴ 660
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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
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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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2.4k
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Answer: A: Is Kallisto Sleuth pipeline suitable for all organisms?
5.6 years ago by prasundutta87 ▴ 660
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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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2.6k
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Answer: A: gffread query for gff to gtf conversion
5.7 years ago by prasundutta87 ▴ 660
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7.0k
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Answer: A: How to extract reads with a known variant form a bam file
6.4 years ago by prasundutta87 ▴ 660
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4.7k
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Answer: A: annotating strand orientation
6.5 years ago by prasundutta87 ▴ 660
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32k
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Answer: Answer: extract only geneID and gene symbol from GTF file
updated 14 months ago by 43k • written 6.5 years ago by ▴ 660
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1.3k
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Answer: C: How to find nu. of variants present in a gene for my Exome seq. sample
6.6 years ago by prasundutta87 ▴ 660
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4.0k
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Answer: A: Calculate the Quality of Bases
6.7 years ago by prasundutta87 ▴ 660
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2.6k
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Answer: A: Mismatch and Indel rate in alignment
6.7 years ago by prasundutta87 ▴ 660
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4.3k
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Answer: A: Keep one SNP for duplicate SNPs
6.7 years ago by prasundutta87 ▴ 660
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1.7k
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Answer: A: Molecular Docking, More Receptors, Single ligand
6.7 years ago by prasundutta87 ▴ 660
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5.9k
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Answer: A: GATK ASEReadCounter: Downstream analysis for identifying allele specific express
6.7 years ago by prasundutta87 ▴ 660
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0
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2.3k
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Answer: A: Ligand Docking Simulation Programs
6.7 years ago by prasundutta87 ▴ 660
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4.8k
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Answer: A: Retrieving SMILES using CAS or SAMPLE ID or SAMPLE_NAME
6.7 years ago by prasundutta87 ▴ 660
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1
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8.0k
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Answer: A: How to get fasta sequences of features from a GFF3 file?
6.7 years ago by prasundutta87 ▴ 660
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2.1k
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Answer: A: SNPEFF for de novo transcriptome annotation
6.8 years ago by prasundutta87 ▴ 660
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2
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2.2k
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Answer: A: difference in genotypes in a multisample vcf file
7.2 years ago by prasundutta87 ▴ 660
38 results • Page 1 of 1
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