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9
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Answer: Answer: Checking Version of Bioconductor
updated 10 weeks ago by 37k • written 5.0 years ago by ▴ 580
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0
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14k
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Answer: A: bedtools coverage gives error received illegal bin number, but that number isn't
updated 4.1 years ago by 37k • written 5.5 years ago by ▴ 580
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1
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2.5k
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Answer: A: tophat aligns to wrong strand
6.1 years ago by apa@stowers ▴ 580
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51k
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Answer: C: Error in read.table(file = file, header = header, sep = sep, quote = quote, :
6.1 years ago by apa@stowers ▴ 580
2
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0
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2.9k
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Answer: A: Data resources for Chromatin accessibility (DNAse, FAIRE, ATAC - seq) and Transc
6.1 years ago by apa@stowers ▴ 580
0
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3.1k
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Answer: A: RNAseq read depth
6.1 years ago by apa@stowers ▴ 580
1
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1
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12k
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Answer: A: Convert read counts to RPKM or TPM values: Numbers don't look right?
6.1 years ago by apa@stowers ▴ 580
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1.2k
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Answer: A: How To Fetch Chromosome Coordinates From Sequence
6.1 years ago by apa@stowers ▴ 580
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0
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2.4k
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Answer: A: genomeCoverageBed : for fixed size bins
6.1 years ago by apa@stowers ▴ 580
2
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0
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2.0k
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Answer: A: miRNA binding detection from RNA-seq reads
6.1 years ago by apa@stowers ▴ 580
1
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1
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3.1k
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Answer: A: miRNA blast to RNA database?
6.1 years ago by apa@stowers ▴ 580
1
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1
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5.2k
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Answer: A: Alignment stats summary by STAR aligner, please help!
6.1 years ago by apa@stowers ▴ 580
4
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1
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15k
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Answer: A: Checking fastq is valid
6.1 years ago by apa@stowers ▴ 580
0
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1
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1.5k
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Answer: A: TF motif half-site enrichment
6.1 years ago by apa@stowers ▴ 580
1
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0
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1.2k
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Answer: A: Screen reads based on certain sequences. Write code myself or designated tools.
6.1 years ago by apa@stowers ▴ 580
1
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0
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1.6k
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Answer: A: Getting plant full length cDNA sequences from NCBI
6.1 years ago by apa@stowers ▴ 580
5
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1
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11k
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Answer: A: Difference between the Fasta files from UCSC and Gencode/Ensembl
6.1 years ago by apa@stowers ▴ 580
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0
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4.1k
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Answer: A: mutations' effect on secondary structure
6.1 years ago by apa@stowers ▴ 580
1
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0
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2.7k
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Answer: A: mapping read is low for miRNA data after trimming
6.1 years ago by apa@stowers ▴ 580
1
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0
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5.4k
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Answer: A: Mapping miRNA to the Human Genome with Bowtie2
6.1 years ago by apa@stowers ▴ 580
1
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0
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7.7k
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Answer: A: Chip-Seq merging peak files
6.1 years ago by apa@stowers ▴ 580
0
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0
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2.0k
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Answer: A: Metrics to evaluate tree congruence
6.1 years ago by apa@stowers ▴ 580
0
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1
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1.5k
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Answer: A: TF motif half-site enrichment
6.1 years ago by apa@stowers ▴ 580
0
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1
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1.4k
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Answer: A: How to calculate the number of proteins present in each chromosomes?
6.1 years ago by apa@stowers ▴ 580
1
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0
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5.3k
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Answer: A: Creating design matrix in LIMMA
6.1 years ago by apa@stowers ▴ 580
1
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0
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4.8k
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Answer: A: How Does Ucsc Liftover Handle Loci That Map To Multiple Genome Positions?
6.1 years ago by apa@stowers ▴ 580
0
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0
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1.7k
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Answer: A: Functional annotation of unigenes
6.1 years ago by apa@stowers ▴ 580
1
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1
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2.0k
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Answer: A: aligning scaffolds to the reference genome
6.1 years ago by apa@stowers ▴ 580
2
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0
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4.0k
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Answer: A: What is the minimum coverage adequate for variant calls from Whole Genome Sequen
6.1 years ago by apa@stowers ▴ 580
2
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1
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2.1k
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Answer: A: lift coordinates mapping to_alt chromosomes in hg38
6.1 years ago by apa@stowers ▴ 580
3
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1
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2.7k
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Answer: A: Yeast GTF file needed for RNA-SeQC run
6.1 years ago by apa@stowers ▴ 580
8
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1
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6.3k
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Answer: A: Is There Any Reason To Do De Novo Transcript Assembly If A Reference Is Availabl
10.9 years ago by apa@stowers ▴ 580
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