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1
vote
0
replies
1.6k
views
Answer:
A: Different NGS runs for paired samples
5.6 years ago by
swbarnes2
15k
1
vote
0
replies
1.8k
views
Comment:
C: How to add annotation for differentially expressed genes obtained using DESeq2
5.6 years ago by
swbarnes2
15k
0
votes
1
reply
1.8k
views
Comment:
C: How to add annotation for differentially expressed genes obtained using DESeq2
5.6 years ago by
swbarnes2
15k
0
votes
0
replies
1.4k
views
Answer:
A: Integrated analysis of TKI-treated and untreated PBMCs - gene expression & vdj l
5.6 years ago by
swbarnes2
15k
0
votes
0
replies
2.9k
views
Answer:
A: Run Cellranger Count with Novogene fastq files
5.6 years ago by
swbarnes2
15k
0
votes
0
replies
4.5k
views
Answer:
A: CellRanger scRNA .mtx only uses 15% of reads in .bam?
5.6 years ago by
swbarnes2
15k
0
votes
1
reply
4.5k
views
Comment:
C: CellRanger scRNA .mtx only uses 15% of reads in .bam?
5.6 years ago by
swbarnes2
15k
0
votes
1
reply
2.6k
views
Answer:
A: there is an error after samtools index
5.6 years ago by
swbarnes2
15k
0
votes
1
reply
3.5k
views
Answer:
A: How to cat fastq files but keep different samples separate
5.6 years ago by
swbarnes2
15k
2
votes
1
reply
7.1k
views
Answer:
A: BWA-MEM read groups usage
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
885
views
Answer:
A: Explaining relation of WGS and transcriptome
5.7 years ago by
swbarnes2
15k
1
vote
0
replies
2.0k
views
Answer:
A: Unbiased clustering from bulk tissue RNA-seq?
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
1.1k
views
Comment:
C: Human DNA - Sequenced by Multiple Labs
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
1.1k
views
Comment:
C: searching for specific RNA nucleotide sequences
5.7 years ago by
swbarnes2
15k
1
vote
0
replies
5.3k
views
Answer:
A: STAR error: EXITING because of FATAL ERROR in reads input: short read sequence l
5.7 years ago by
swbarnes2
15k
3
votes
1
reply
11k
views
Answer:
C: Illumina index adapter trimming of FASTQ files using Cutadapt/TrimGalore
5.7 years ago by
swbarnes2
15k
0
votes
0
replies
12k
views
Comment:
C: How to split fastq file containing Forward and Reverse reads to two files Forwar
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
12k
views
Comment:
C: How to split fastq file containing Forward and Reverse reads to two files Forwar
5.7 years ago by
swbarnes2
15k
0
votes
0
replies
769
views
Answer:
A: Can I add the read counts to the re-sequenced read counts directly?
5.7 years ago by
swbarnes2
15k
1
vote
1
reply
3.0k
views
Comment:
C: Salmon annotation of transcripts in quasi-mapping step
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
1.4k
views
Comment:
C: How to make some modifications to reference genome?
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
1.9k
views
Answer:
A: Compute Mapping quality for invariant sites
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
2.9k
views
Comment:
C: something strange when use UMI-tools dedup&count after STAR alignment
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
2.9k
views
Comment:
C: something strange when use UMI-tools dedup&count after STAR alignment
5.7 years ago by
swbarnes2
15k
0
votes
2
replies
2.1k
views
Answer:
A: Strange coverage of mtDNA - need help interpreting MiSeq results
5.7 years ago by
swbarnes2
15k
0
votes
0
replies
2.4k
views
Answer:
A: combining reads from multiple lanes for DE analysis
5.7 years ago by
swbarnes2
15k
0
votes
0
replies
5.0k
views
Comment:
C: How to get different outputs for kallisto on multiple samples?
5.7 years ago by
swbarnes2
15k
0
votes
2
replies
12k
views
Answer:
A: How to normalize gene expression with CPM
5.7 years ago by
swbarnes2
15k
0
votes
1
reply
5.0k
views
Answer:
A: How to get different outputs for kallisto on multiple samples?
5.7 years ago by
swbarnes2
15k
0
votes
0
replies
1.7k
views
Answer:
A: Replacing BAM reference
5.7 years ago by
swbarnes2
15k
2
votes
0
replies
1.7k
views
Comment:
C: Replacing BAM reference
5.7 years ago by
swbarnes2
15k
1
vote
0
replies
1.9k
views
Comment:
C: Pros and cons to do biomedical research in pharmaceutical company
5.8 years ago by
swbarnes2
15k
1
vote
0
replies
1.6k
views
Answer:
A: Excel: using quartiles & averageifs to combine probe values without outliers
5.8 years ago by
swbarnes2
15k
0
votes
1
reply
2.3k
views
Comment:
C: Are there any issues with using sample reads coming from different technologies
5.8 years ago by
swbarnes2
15k
0
votes
0
replies
1.8k
views
Answer:
A: HISAT2 on multiple samples
5.8 years ago by
swbarnes2
15k
1
vote
1
reply
2.8k
views
Answer:
A: umi_tools count omitting majority of reads
5.8 years ago by
swbarnes2
15k
0
votes
0
replies
1.2k
views
Answer:
A: about the batch effects
5.8 years ago by
swbarnes2
15k
1
vote
0
replies
1.7k
views
Answer:
A: Extract subsequences from a fastA file with specific start sequence and length i
5.8 years ago by
swbarnes2
15k
1
vote
1
reply
3.0k
views
Comment:
C: How to analyze this kind format of 10x single cell RNA-seq data?
5.8 years ago by
swbarnes2
15k
0
votes
1
reply
3.0k
views
Comment:
C: How to analyze this kind format of 10x single cell RNA-seq data?
5.8 years ago by
swbarnes2
15k
2
votes
1
reply
3.0k
views
Comment:
C: How to analyze this kind format of 10x single cell RNA-seq data?
5.8 years ago by
swbarnes2
15k
1
vote
1
reply
1.4k
views
Answer:
A: Complex DESeq2 Model with different gene dosages
5.8 years ago by
swbarnes2
15k
1
vote
0
replies
4.9k
views
Answer:
A: best way to combine RNAseq data from different sequencing batches
5.8 years ago by
swbarnes2
15k
0
votes
0
replies
1.8k
views
Answer:
A: Is it Possible to Filter a sc-RNA-Seq FASTQ based Upon Known Cell Barcodes?
5.8 years ago by
swbarnes2
15k
0
votes
0
replies
3.0k
views
Comment:
C: configure of bcl2fastq
5.8 years ago by
swbarnes2
15k
1
vote
1
reply
1.7k
views
Comment:
C: design matrix dseq2
5.8 years ago by
swbarnes2
15k
0
votes
1
reply
3.0k
views
Comment:
C: configure of bcl2fastq
5.8 years ago by
swbarnes2
15k
0
votes
1
reply
1.7k
views
Answer:
A: design matrix dseq2
5.8 years ago by
swbarnes2
15k
0
votes
0
replies
4.6k
views
Comment:
C: What do I need to do in order to use multiple different reference genomes when a
5.8 years ago by
swbarnes2
15k
2
votes
1
reply
4.6k
views
Answer:
A: What do I need to do in order to use multiple different reference genomes when a
5.8 years ago by
swbarnes2
15k
2,124 results • Page
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