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Comment: C: Setting/finding the log odds detection threshold in custom homer PWMs
4.2 years ago by tiago211287 ★ 1.5k
0
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1
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2.6k
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Comment: C: Unzipping SAM files
updated 4.2 years ago by 44k • written 4.2 years ago by ★ 1.5k
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0
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6.0k
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Comment: C: What is difference between bulk RNAseq and mRNAseq?
4.2 years ago by tiago211287 ★ 1.5k
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2
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6.0k
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Comment: C: What is difference between bulk RNAseq and mRNAseq?
4.2 years ago by tiago211287 ★ 1.5k
0
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0
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1.5k
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Comment: C: Denovo assembly or Reference based assembly for identifying novel lncRNAs
4.2 years ago by tiago211287 ★ 1.5k
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1
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1.5k
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Comment: C: How can I add sequences to my BED file?
4.2 years ago by tiago211287 ★ 1.5k
0
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1
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971
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Answer: A: Differential Gene Expression Using Deseq2
4.2 years ago by tiago211287 ★ 1.5k
2
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2.0k
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Answer: A: multi-factor Deseq LRT test analysis
4.2 years ago by tiago211287 ★ 1.5k
0
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1
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2.0k
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Answer: A: Cellranger: BCR analysis
4.2 years ago by tiago211287 ★ 1.5k
0
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1
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5.4k
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Comment: C: Counting single-cell ATAC fragments at peaks on BED file
4.4 years ago by tiago211287 ★ 1.5k
4
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1
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2.0k
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Comment: C: enhanced volcano plot
4.4 years ago by tiago211287 ★ 1.5k
15
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7
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2.5k
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Can Tophat2 Align a Book?
Tophat2
updated 23 months ago by 44k • written 9.4 years ago by ★ 1.5k
1
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1
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2.4k
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Comment: C: block design with time course and DESeq2
updated 4.9 years ago by 44k • written 8.8 years ago by ★ 1.5k
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0
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5.5k
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Comment: C: How can I know what genes each Trinity ID are ?
updated 4.9 years ago by 44k • written 8.9 years ago by ★ 1.5k
2
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1
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4.9k
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Answer: Answer: How to separate htseq-count table to coding RNAs and non-coding RNAs
updated 2.2 years ago by 44k • written 9.2 years ago by ★ 1.5k
4
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0
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66k
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Answer: A: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 5.0 years ago by 44k • written 9.3 years ago by ★ 1.5k
0
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2
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12k
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Comment: C: how to extract the genomic positions and chromosome number for a list of genes
5.7 years ago by tiago211287 ★ 1.5k
0
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1
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12k
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Comment: C: how to extract the genomic positions and chromosome number for a list of genes
5.7 years ago by tiago211287 ★ 1.5k
0
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1
reply
12k
views
Comment: C: how to extract the genomic positions and chromosome number for a list of genes
5.7 years ago by tiago211287 ★ 1.5k
6
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1
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12k
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Answer: Answer: how to extract the genomic positions and chromosome number for a list of genes
updated 18 months ago by 44k • written 5.7 years ago by ★ 1.5k
3
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0
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2.0k
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Comment: C: Bioinformatics question regarding multilevel pie chart
5.8 years ago by tiago211287 ★ 1.5k
1
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1
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15k
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Comment: C: ATAC-seq DE analysis
6.0 years ago by tiago211287 ★ 1.5k
0
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0
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2.8k
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Comment: C: bam file merge
6.4 years ago by tiago211287 ★ 1.5k
0
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1
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9.8k
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Comment: C: Filtering rRNA from RNAseq data
6.4 years ago by tiago211287 ★ 1.5k
0
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1
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925
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Comment: C: want to pick up the strongest peaks in all the duplicates
6.4 years ago by tiago211287 ★ 1.5k
0
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0
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4.0k
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Comment: C: How to use GNU parallel to download SRA files
6.8 years ago by tiago211287 ★ 1.5k
1
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1
reply
2.8k
views
Comment: C: Using Bowtie-2 for global (genome) sequence alignment
6.8 years ago by tiago211287 ★ 1.5k
0
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0
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3.6k
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Comment: C: How long does it take to map a data of 800 MB using STAR ?
6.8 years ago by tiago211287 ★ 1.5k
1
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0
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5.7k
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Comment: C: i meet an error when i run the cuffmerge
6.8 years ago by tiago211287 ★ 1.5k
2
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0
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12k
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Answer: A: How to remove duplicate sequences in fasta file using python?
6.8 years ago by tiago211287 ★ 1.5k
1
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0
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9.8k
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Comment: C: Too many differentially expressed genes in RNA-seq?
6.8 years ago by tiago211287 ★ 1.5k
0
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1
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4.0k
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Comment: C: How to use GNU parallel to download SRA files
6.8 years ago by tiago211287 ★ 1.5k
3
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1
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4.0k
views
Answer: A: How to use GNU parallel to download SRA files
updated 6.8 years ago by 147k • written 6.8 years ago by ★ 1.5k
6
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0
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20k
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Answer: C: How to count fasta sequences efficiently using (or not ) biopython
6.8 years ago by tiago211287 ★ 1.5k
2
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0
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9.8k
views
Answer: A: Too many differentially expressed genes in RNA-seq?
6.8 years ago by tiago211287 ★ 1.5k
0
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0
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3.1k
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Answer: C: how to give limitation in heatmap3
6.8 years ago by tiago211287 ★ 1.5k
2
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1
reply
19k
views
Comment: C: Nextera Transposon Contamination
6.8 years ago by tiago211287 ★ 1.5k
1
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0
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9.3k
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Answer: A: pathway for single cell RNA-seq
6.8 years ago by tiago211287 ★ 1.5k
1
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1
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1.3k
views
Answer: A: how to get common variants between two species?
6.8 years ago by tiago211287 ★ 1.5k
1
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0
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9.3k
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Comment: C: pathway for single cell RNA-seq
6.8 years ago by tiago211287 ★ 1.5k
2
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1
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1.5k
views
Answer: A: Tools for asserting matching pairs of samples from the same patient
6.8 years ago by tiago211287 ★ 1.5k
0
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0
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10k
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Comment: C: Position Weight Matrix From Sequence Alignment
7.0 years ago by tiago211287 ★ 1.5k
0
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1
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5.5k
views
Comment: C: Command or Perl script for changing headers of multiple FASTA files in a specifi
7.2 years ago by tiago211287 ★ 1.5k
1
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1
reply
5.5k
views
Answer: A: Command or Perl script for changing headers of multiple FASTA files in a specifi
7.2 years ago by tiago211287 ★ 1.5k
0
votes
1
reply
5.5k
views
Comment: C: Command or Perl script for changing headers of multiple FASTA files in a specifi
7.2 years ago by tiago211287 ★ 1.5k
0
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1
reply
5.5k
views
Comment: C: Command or Perl script for changing headers of multiple FASTA files in a specifi
7.2 years ago by tiago211287 ★ 1.5k
1
vote
0
replies
11k
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Answer: A: Downloading the latest human genome
7.2 years ago by tiago211287 ★ 1.5k
1
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0
replies
9.3k
views
Comment: C: Demultiplexing reads with index present in the labels
7.2 years ago by tiago211287 ★ 1.5k
12
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2
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9.3k
views
Demultiplexing reads with index present in the labels
demultiplex illumina index rnaseq
7.2 years ago by tiago211287 ★ 1.5k
0
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0
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9.9k
views
Comment: C: How to split a fastq file into each corresponding sample.fastq?
7.2 years ago by tiago211287 ★ 1.5k
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