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Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
5 days ago by
BioinfGuru
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Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
5 days ago by
BioinfGuru
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Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
5 days ago by
BioinfGuru
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Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
5 days ago by
BioinfGuru
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Comment: Installing/switching between versions of R/Rstudio/Bioconductor on personal mach
5 days ago by
BioinfGuru
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Comment: Installing/switching between versions of R/Rstudio/Bioconductor
5 days ago by
BioinfGuru
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688
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Comment: RNA seq differential expression analysis
5 days ago by
BioinfGuru
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616
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Comment: DEG analysis of RNA-seq data across multiple tissues and two conditions
6 days ago by
BioinfGuru
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616
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Comment: DEG analysis of RNA-seq data across multiple tissues and two conditions
7 days ago by
BioinfGuru
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857
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Comment: RNAseq of primary tumor and metastases in two different organ
8 days ago by
BioinfGuru
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857
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Comment: RNAseq of primary tumor and metastases in two different organ
8 days ago by
BioinfGuru
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222
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Comment: gene body coverage with RSeqQC
8 days ago by
BioinfGuru
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2
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277
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Comment: Bioinformatics_where do i start
8 days ago by
BioinfGuru
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857
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Comment: RNAseq of primary tumor and metastases in two different organ
8 days ago by
BioinfGuru
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857
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Comment: RNAseq of primary tumor and metastases in two different organ
8 days ago by
BioinfGuru
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857
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Comment: RNAseq of primary tumor and metastases in two different organ
12 days ago by
BioinfGuru
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386
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Comment: what is the normal range of htseq-count output for homo sapiens RNA-Seq
12 days ago by
BioinfGuru
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646
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Comment: Help with summarizeOverlaps function in RNASeq analysis using R
17 days ago by
BioinfGuru
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646
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Comment: Help with summarizeOverlaps function in RNASeq analysis using R
17 days ago by
BioinfGuru
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278
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Comment: Removing batch effect using combat-seq
23 days ago by
BioinfGuru
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278
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Comment: Removing batch effect using combat-seq
24 days ago by
BioinfGuru
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646
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Comment: Help with summarizeOverlaps function in RNASeq analysis using R
25 days ago by
BioinfGuru
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646
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Comment: Help with summarizeOverlaps function in RNASeq analysis using R
25 days ago by
BioinfGuru
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446
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Comment: How do I get the gene annotations as a text file from a genebank file?
27 days ago by
BioinfGuru
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1.1k
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Comment: What is the sequence origin in human plasma?
4 weeks ago by
BioinfGuru
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259
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Comment: PCA script correction
4 weeks ago by
BioinfGuru
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513
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Comment: Searching for gene in multiple genomes
4 weeks ago by
BioinfGuru
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1.1k
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Comment:
Comment: What is the sequence origin in human plasma?
4 weeks ago by
BioinfGuru
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475
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Comment: RNA-seq differential expression across multiple tissues, 2 trials, and 2 conditi
5 weeks ago by
BioinfGuru
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279
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Comment: What GC content should I expect?
5 weeks ago by
BioinfGuru
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342
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Comment: How do I collapse rows of a tibble in R?
6 weeks ago by
BioinfGuru
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911
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Comment: How to download multiple .gz files from Ensembl Protists database
9 weeks ago by
BioinfGuru
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Comment: How to get the chromosome numbers from RefSeq accession IDs?
9 weeks ago by
BioinfGuru
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284
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Comment: RNA-Seq | DESeq2 | differentially expressed genes | Dispersion
10 weeks ago by
BioinfGuru
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0
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5.7k
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Comment:
C: Quantile normalisation: raw rpkm or log2rpkm?
updated 5.2 years ago by
Ram
43k • written 7.5 years ago by
BioinfGuru
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1.4k
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Comment:
C: Can i use ucsc track browser without a reference organism?
5.6 years ago by
BioinfGuru
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1.4k
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Comment:
C: Can i use ucsc track browser without a reference organism?
5.6 years ago by
BioinfGuru
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6.9k
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Comment:
C: mitochondrial blacklists ATAC-Seq
updated 5.6 years ago by
Ram
43k • written 7.1 years ago by
BioinfGuru
★ 1.7k
1
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1
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4.7k
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Comment:
C: Confused about merging RNA-seq lanes/runs
5.9 years ago by
BioinfGuru
★ 1.7k
1
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2
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4.7k
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Comment:
C: Can we concatenate two fastq files from same sample but different runs
5.9 years ago by
BioinfGuru
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6.6k
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Comment:
C: Picard MarkDuplicates flag vs remove issue
5.9 years ago by
BioinfGuru
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1.9k
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Comment:
C: Is the sequence quality good enough?
5.9 years ago by
BioinfGuru
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1.9k
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Comment:
C: Is the sequence quality good enough?
5.9 years ago by
BioinfGuru
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0
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1.9k
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Comment:
C: Is the sequence quality good enough?
5.9 years ago by
BioinfGuru
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1
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0
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2.1k
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Comment:
C: Low mapping percentage after mapping RNA-seq reads to a closely related species
5.9 years ago by
BioinfGuru
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0
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2.4k
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Comment:
C: HaplotypeCaller output - All records are non-variant - Have I gone wrong somwher
5.9 years ago by
BioinfGuru
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2
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1
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12k
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Comment:
C: How to select an aligner?
5.9 years ago by
BioinfGuru
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3.0k
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Comment:
C: Parsing Blast output on linux/unix
5.9 years ago by
BioinfGuru
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0
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2.8k
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Comment:
C: GATK SNPs calling multiple sample without any known SNPs database
5.9 years ago by
BioinfGuru
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2
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1
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2.0k
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Comment:
C: location of mutations
5.9 years ago by
BioinfGuru
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