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Comment: Comment: HTseq no features
13 months ago by michael.ante ★ 3.8k
1
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0
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965
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Comment: Comment: RNA seq for different tissues samples
16 months ago by michael.ante ★ 3.8k
0
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1
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819
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Comment: Comment: finding overlapping motifs to increase length of motif
17 months ago by michael.ante ★ 3.8k
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0
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429
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Comment: Comment: Quantify gene expression using flanking sequences
19 months ago by michael.ante ★ 3.8k
1
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0
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2.1k
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Comment: Comment: Searching for mRNA ending with a specific 3' pattern in NON-poly-A RNASeq data.
2.6 years ago by michael.ante ★ 3.8k
0
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1
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2.1k
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Comment: C: How to extract sequences from multiple fastq files based on part of the header?
3.1 years ago by michael.ante ★ 3.8k
1
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0
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773
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Comment: C: How to interpret one region of gene with much higher RNASeq coverage than other
3.1 years ago by michael.ante ★ 3.8k
0
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0
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1.5k
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Comment: C: How to identify 3'UTR region?
4.2 years ago by michael.ante ★ 3.8k
0
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0
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1.6k
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Comment: C: featureCounts log: "WARNING contig is not found in the provided genome file!"
4.2 years ago by michael.ante ★ 3.8k
0
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0
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1.1k
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Comment: C: Would curated pathway gene set better being weighted than being binary
4.3 years ago by michael.ante ★ 3.8k
0
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1
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1.1k
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Comment: C: Would curated pathway gene set better being weighted than being binary
4.3 years ago by michael.ante ★ 3.8k
0
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0
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1.9k
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Comment: C: Extract sequences from fastA files based on csv chart in R
4.3 years ago by michael.ante ★ 3.8k
0
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1
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1.9k
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Comment: C: Extract sequences from fastA files based on csv chart
4.3 years ago by michael.ante ★ 3.8k
0
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0
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1.7k
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Comment: C: Error in piRNA gtf file while featurecounts step in STAR aligner?
4.3 years ago by michael.ante ★ 3.8k
0
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1
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1.5k
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Comment: C: STAR error (segmentation fault) in Aligning reads
4.3 years ago by michael.ante ★ 3.8k
0
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2
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2.0k
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Comment: C: FASTQ exctract ID's
4.3 years ago by michael.ante ★ 3.8k
1
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1
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1.5k
views
Comment: C: STAR error (segmentation fault) in Aligning reads
4.3 years ago by michael.ante ★ 3.8k
0
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0
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995
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Comment: C: Data set containing corresponding RNA-seq and RT-Qpcr data
4.3 years ago by michael.ante ★ 3.8k
0
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1
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2.8k
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Comment: C: bash loop to count variants using vcftools
updated 4.4 years ago by 43k • written 8.4 years ago by ★ 3.8k
0
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0
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2.1k
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Comment: C: RNA-SeQC v1.1.8 transcript_id attribute was not found
4.4 years ago by michael.ante ★ 3.8k
1
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0
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6.4k
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Comment: C: How to confirm forward primer matches each read without removing primer sequence
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
2
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1
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31k
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Comment: C: getting intersect between two lists of genes in R
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
1
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1
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31k
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Comment: C: getting intersect between two lists of genes in R
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
1
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1
reply
31k
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Comment: C: getting intersect between two lists of genes in R
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
0
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1
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4.1k
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Comment: C: Annotating RNA-Seq exon junctions
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
3
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1
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4.4k
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Comment: C: Merge 2 files based on rs number but keep all info only from the first file
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 3.8k
0
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0
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2.3k
views
Comment: C: Nothing will align with HTSeq?
updated 4.4 years ago by 43k • written 8.6 years ago by ★ 3.8k
2
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1
reply
6.6k
views
Comment: C: Using featureCount with a GFF file
4.4 years ago by michael.ante ★ 3.8k
1
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1
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6.6k
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Comment: C: Using featureCount with a GFF file
4.4 years ago by michael.ante ★ 3.8k
0
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1
reply
7.2k
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Comment: C: Removing barcode and adapters?
updated 4.5 years ago by 43k • written 8.8 years ago by ★ 3.8k
0
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0
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7.7k
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Comment: C: Bedtools problem : It looks as though you have less than 3 columns at line: 1.
4.5 years ago by michael.ante ★ 3.8k
1
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0
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3.9k
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Comment: C: salmon was only able to assign 0 fragments to transcripts
4.5 years ago by michael.ante ★ 3.8k
0
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1
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2.0k
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Comment: C: awk, copy and paste single line command
4.5 years ago by michael.ante ★ 3.8k
1
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0
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3.2k
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Comment: C: bbduk flags 'tossbrokenreads' and 'nullifybrokenquality'
4.5 years ago by michael.ante ★ 3.8k
0
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1
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3.2k
views
Comment: A: bbduk flags 'tossbrokenreads' and 'nullifybrokenquality'
4.5 years ago by michael.ante ★ 3.8k
0
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0
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1.6k
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Comment: C: Are reads with the same length and position always "duplicates"
4.5 years ago by michael.ante ★ 3.8k
0
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1
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1.6k
views
Comment: C: can I use soft-clip RNA-seq reads to summarize gene counts?
4.5 years ago by michael.ante ★ 3.8k
2
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1
reply
2.3k
views
Comment: Comment: Which tool/method to use for Raw data quality evaluation and filtering
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 3.8k
0
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0
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6.0k
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Comment: C: Count matrix from bigwig files - Application
4.5 years ago by michael.ante ★ 3.8k
1
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0
replies
1.2k
views
Comment: C: How to calculate the number of functional proteins in GFF3 file
4.5 years ago by michael.ante ★ 3.8k
0
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1
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2.0k
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Comment: C: STAR output soft-clipped reads instead of insertion
4.5 years ago by michael.ante ★ 3.8k
2
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1
reply
3.5k
views
Comment: C: STAR aligner maps 0 reads to multiple loci, but 3.7% to too many loci - meaning?
4.5 years ago by michael.ante ★ 3.8k
1
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1
reply
1.2k
views
Comment: C: How to calculate the number of functional proteins in GFF3 file
4.5 years ago by michael.ante ★ 3.8k
1
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0
replies
1.9k
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Comment: C: Question about featureCounts
4.5 years ago by michael.ante ★ 3.8k
0
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0
replies
1.9k
views
Comment: C: Reverse Complement Reads in BAM File
4.5 years ago by michael.ante ★ 3.8k
1
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0
replies
1.8k
views
Comment: C: Stringtie and prepDE
4.5 years ago by michael.ante ★ 3.8k
0
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1
reply
2.0k
views
Comment: C: Clipping primer after alignment
4.6 years ago by michael.ante ★ 3.8k
1
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0
replies
809
views
Comment: C: General guidance with project about gene duplication
4.6 years ago by michael.ante ★ 3.8k
1
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0
replies
1.0k
views
Comment: C: HT-seq-count default parameter to "score"secondary alignments contradicts its do
4.6 years ago by michael.ante ★ 3.8k
0
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1
reply
2.9k
views
Comment: C: Converting and sorting .sam at the same time
4.6 years ago by michael.ante ★ 3.8k
249 results • Page 1 of 5
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