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Comment: C: BLAT with cython? Bypassing the IO of BLAT
9.4 years ago by Devon Ryan 105k
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1.7k
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Comment: C: Width setting in r
9.4 years ago by Devon Ryan 105k
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Answer: A: Width setting in r
9.4 years ago by Devon Ryan 105k
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2.8k
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Comment: C: BLAT with cython? Bypassing the IO of BLAT
9.4 years ago by Devon Ryan 105k
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2.2k
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Comment: C: Same pathways between different diseases
9.4 years ago by Devon Ryan 105k
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2.8k
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Comment: C: How does SNP position numeration work?
9.4 years ago by Devon Ryan 105k
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7.0k
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Comment: C: How long it takes to run repeat masker on a full genome
9.4 years ago by Devon Ryan 105k
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7.0k
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Comment: C: How long it takes to run repeat masker on a full genome
9.4 years ago by Devon Ryan 105k
3
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2.9k
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Answer: A: Biggest barriers to making sense of sequence data
9.4 years ago by Devon Ryan 105k
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5.3k
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Answer: A: Coverage-search vs. no coverage-search in running Tophat
9.4 years ago by Devon Ryan 105k
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9.8k
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Comment: C: Should I remove Kmers identified in FastQC?
9.4 years ago by Devon Ryan 105k
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8.4k
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Comment: C: extracting reads from fastq file based on read_id
9.4 years ago by Devon Ryan 105k
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5.5k
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Comment: C: Question about RRBS mapping efficiency
9.4 years ago by Devon Ryan 105k
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5.5k
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Comment: C: Question about RRBS mapping efficiency
9.4 years ago by Devon Ryan 105k
3
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5.5k
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Answer: A: Question about RRBS mapping efficiency
9.4 years ago by Devon Ryan 105k
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2.1k
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Comment: C: Any paper or journal review about repeated multiple testing for ChIP-seq replica
9.4 years ago by Devon Ryan 105k
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2.1k
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Comment: C: Any paper or journal review about repeated multiple testing for ChIP-seq replica
9.4 years ago by Devon Ryan 105k
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2.5k
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Comment: C: Finding DEGs using RNA-seq data
9.4 years ago by Devon Ryan 105k
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1.8k
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Comment: C: htseq-count actual reads number is different with the result.
9.4 years ago by Devon Ryan 105k
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2.5k
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Answer: A: Finding DEGs using RNA-seq data
9.4 years ago by Devon Ryan 105k
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2.6k
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Comment: C: Significance within conditions
9.4 years ago by Devon Ryan 105k
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1
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8.6k
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Comment: C: read trimming for small RNA NGS data
9.4 years ago by Devon Ryan 105k
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8.6k
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Comment: C: read trimming for small RNA NGS data
9.4 years ago by Devon Ryan 105k
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4.8k
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Comment: C: MNase-seq / fragment size selection
9.4 years ago by Devon Ryan 105k
3
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4.8k
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Answer: A: MNase-seq / fragment size selection
9.4 years ago by Devon Ryan 105k
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1.6k
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Comment: C: Tool for Variant Normalization nomenclature
9.4 years ago by Devon Ryan 105k
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1
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1.6k
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Answer: A: Tool for Variant Normalization nomenclature
9.4 years ago by Devon Ryan 105k
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4.1k
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Comment: C: Rembrandt Glioma Data Analysis (PART I) - Are Gender specific genes related to c
9.4 years ago by Devon Ryan 105k
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2.5k
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Comment: C: How can I select reads Based on the best MAPQ and exclude reads with the same na
9.4 years ago by Devon Ryan 105k
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1
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2.5k
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Answer: A: How can I select reads Based on the best MAPQ and exclude reads with the same na
9.4 years ago by Devon Ryan 105k
1
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1
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8.6k
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Comment: C: Paired End FASTQ data; separate files for reverse forward strand reads?
9.4 years ago by Devon Ryan 105k
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1.6k
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Comment: C: Gene expression abundance data
9.4 years ago by Devon Ryan 105k
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1
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1.8k
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Comment: C: Any package in R for imputing missing values based on GO ontology?
9.4 years ago by Devon Ryan 105k
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5.7k
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Comment: C: How to subsample reads for a chromosome in a BAM file with samtools?
9.4 years ago by Devon Ryan 105k
1
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2.6k
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Comment: C: ChIP-seq normalization, Signal-to-Noise different between samples
9.4 years ago by Devon Ryan 105k
1
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1
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2.5k
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Comment: C: What is the genic size (exon+intron) of a genome
9.4 years ago by Devon Ryan 105k
3
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1
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5.7k
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Answer: A: How to subsample reads for a chromosome in a BAM file with samtools?
9.4 years ago by Devon Ryan 105k
1
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2.8k
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Comment: C: what is R shiny application is used for and how to load it in a webpage ?
9.4 years ago by Devon Ryan 105k
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1
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6.8k
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Comment: C: Comparing lists of differentially expressed genes
9.4 years ago by Devon Ryan 105k
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2.6k
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Comment: C: Significance within conditions
9.4 years ago by Devon Ryan 105k
2
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2.6k
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Answer: A: Significance within conditions
9.4 years ago by Devon Ryan 105k
0
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3.8k
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Comment: C: How to count number of unique exons/introns (and their locations) in a GTF file?
9.4 years ago by Devon Ryan 105k
3
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2
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6.8k
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Answer: A: Comparing lists of differentially expressed genes
9.4 years ago by Devon Ryan 105k
1
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1
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3.8k
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Comment: C: How to count number of unique exons/introns (and their locations) in a GTF file?
9.4 years ago by Devon Ryan 105k
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0
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12k
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Comment: C: How to identify Gene IDs ?
9.4 years ago by Devon Ryan 105k
1
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2.8k
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Comment: C: Flagstat results: 0 reads
9.4 years ago by Devon Ryan 105k
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0
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5.1k
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Comment: C: why my resultsNames(deseq) is not the same as model.matrix ?
9.4 years ago by Devon Ryan 105k
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1
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5.1k
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Answer: A: why my resultsNames(deseq) is not the same as model.matrix ?
9.4 years ago by Devon Ryan 105k
1
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0
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2.8k
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Answer: C: Illumina NextSeq SampleSheets
9.4 years ago by Devon Ryan 105k
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1
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2.7k
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Comment: C: Is it possible that the control data will be bigger than the treatment samples'
9.4 years ago by Devon Ryan 105k
10,053 results • Page 87 of 202
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