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Comment: C: Using reads for phylogenies
7.1 years ago by h.mon 35k
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2.5k
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Comment: C: 20-mer DNA sequence list - assess similarity
7.1 years ago by h.mon 35k
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1
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2.1k
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Comment: C: why forward reads were much more than reverse reads In strand specific RNAseq d
7.1 years ago by h.mon 35k
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Comment: C: Semicolon vs vertical line separating GO annotations in .go file
7.1 years ago by h.mon 35k
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2.5k
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Comment: C: How can I Rectify Segmentation fault: 11?
7.1 years ago by h.mon 35k
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2.5k
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Answer: A: How can I Rectify Segmentation fault: 11?
7.1 years ago by h.mon 35k
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2.7k
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Comment: C: Use Read ID File to parse out reads from a Fasta File
7.1 years ago by h.mon 35k
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8.2k
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Comment: C: DESeq2 log2 fold change
7.1 years ago by h.mon 35k
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2
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8.8k
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Answer: A: Align paired and unpaired reads simultaneously using Bowtie2?
7.1 years ago by h.mon 35k
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2.7k
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Answer: A: Use Read ID File to parse out reads from a Fasta File
7.1 years ago by h.mon 35k
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4.9k
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Comment: C: While using ggtree in rstudio, it shows error in some commands
7.1 years ago by h.mon 35k
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1.6k
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Answer: A: RNASeq_pipeline.config.sh of HISAT
7.1 years ago by h.mon 35k
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Comment: C: In Enrichr: What is "Gene weight" or "levels of membership"?
7.1 years ago by h.mon 35k
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2.8k
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Answer: A: How to export the SNPs between whole genome alignments using the command line?
7.1 years ago by h.mon 35k
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12k
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Answer: A: Is there consensus on what constitutes a good BUSCO score?
7.1 years ago by h.mon 35k
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1.3k
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Answer: A: R package to annotate and explore effect of biases in RNA Seq
7.1 years ago by h.mon 35k
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2.0k
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Comment: C: RNA-seq High Variation Between and Within Groups
7.1 years ago by h.mon 35k
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2.0k
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Comment: C: Create a GTF file from mapped reads
7.1 years ago by h.mon 35k
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1
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10k
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Answer: A: Rsubread: Aligning multiple paired-end files
7.1 years ago by h.mon 35k
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11k
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Comment: C: what is gc bias?
7.1 years ago by h.mon 35k
1
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0
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by h.mon 35k
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1
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by h.mon 35k
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2.0k
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Comment: C: How to get count matrix from aligned file
7.1 years ago by h.mon 35k
1
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by h.mon 35k
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1.0k
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Answer: A: Using different assemblies to create a whole genome (bacteria)
7.1 years ago by h.mon 35k
3
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13k
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Comment: C: best way to visualize bam file
7.1 years ago by h.mon 35k
4
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2.9k
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Answer: A: DESeq2 - HTSeq-count txt error
7.1 years ago by h.mon 35k
2
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1
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1.7k
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Comment: C: Computation-Intesive Application in the field of bioinformatics
7.1 years ago by h.mon 35k
2
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1.3k
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Answer: A: Differences between parSeqSim and twoSeqSim results
7.1 years ago by h.mon 35k
1
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0
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2.5k
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Answer: A: Directionality of KEGG/Reactome/Wikipathways
7.1 years ago by h.mon 35k
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0
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1.8k
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Answer: A: Help interpreting Stringtie 'fully covered transcripts' output
7.1 years ago by h.mon 35k
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1
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1.8k
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Comment: C: Using mmseq expression data for analysis/classification
7.1 years ago by h.mon 35k
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2.6k
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Comment: C: mice whole genome sequencing Analysis
7.1 years ago by h.mon 35k
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1
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2.1k
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Comment: C: Insert size smaller than the read lenght
7.1 years ago by h.mon 35k
1
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1
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4.9k
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Comment: C: Efficiently aligning a lot of reads on the same small reference sequence
7.1 years ago by h.mon 35k
0
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1
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4.9k
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Comment: C: Efficiently aligning a lot of reads on the same small reference sequence
7.1 years ago by h.mon 35k
1
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0
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4.9k
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Comment: C: Efficiently aligning a lot of reads on the same small reference sequence
updated 7.1 years ago by 11k • written 7.1 years ago by 35k
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2.5k
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Comment: C: which gap filler do you recommend?
7.1 years ago by h.mon 35k
0
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1
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2.5k
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Comment: C: which gap filler do you recommend?
7.1 years ago by h.mon 35k
3
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1
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9.8k
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Answer: A: Very low unique mapped reads - STAR alignment
7.1 years ago by h.mon 35k
3
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0
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2.9k
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Comment: C: How to acknowledge in the paper a reference genome that hasn't been published ye
7.1 years ago by h.mon 35k
0
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1
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2.9k
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Comment: C: How to acknowledge in the paper a reference genome that hasn't been published ye
7.1 years ago by h.mon 35k
0
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1
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12k
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Comment: C: How to get PCA3 and PCA4 from Deseq2?
7.1 years ago by h.mon 35k
1
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0
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3.0k
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Comment: C: Tools for annotating UTRs
7.1 years ago by h.mon 35k
4
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1
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2.2k
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Comment: C: A way to verify that GFF and Fasta files make a valid pair (came from the same p
7.1 years ago by h.mon 35k
4
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0
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12k
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Answer: A: How to get PCA3 and PCA4 from Deseq2?
7.1 years ago by h.mon 35k
2
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1
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1.4k
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Answer: A: Retrieve gene length and cds locus informartion
7.1 years ago by h.mon 35k
0
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0
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2.7k
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Comment: C: Problems running Trinity 2.6.6.
7.1 years ago by h.mon 35k
6
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1
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21k
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Comment: C: Running STAR aligner on paired-end reads as single-end read
7.1 years ago by h.mon 35k
1
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1
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2.1k
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Comment: C: TopHat Error: Couldn't build bowtie index with err = -11
7.1 years ago by h.mon 35k
4,239 results • Page 34 of 85
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