Kallisto M1 Macbook Pro
Trying to run kallisto on new M1 Pro Macbook; 10 core CPU; four paired-end reads in my sample alignment; taking very long time. Is this expected? Am I doing something wrong?
m1
rnaseq
kallisto
mac
• 2,544 views
•
link
updated
by
GenoMax
16K
• |
written
by
ryancaugustin
0
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Illumina sequencing data trimming help
written by Elena 0Hi! I never posted here before but I wanted somebody's opinion. I did paired end Illumina sequencing on mosquito DNA and ran fastqc to check …
-
How to do preprocessing from fastqc
written by Lulu 0Could someone provide a detailed guide on downstream preprocessing steps based on my FASTQC report? I conducted FASTQC analysis on a paired sample, and here …
-
Increasing per base G content in QC sequencing files
written by robertsr 0Hello, I conducted some metagenomic sequencing as follows: - Metagenomic sequencing from human stool samples - PCR-free library prep using NEB kit (450bp insert) - …
-
Multiple threads on ubuntu server
written by oghzzang 5I am using Ubuntu 16.04 server. 88 threads, mem500Gb. I used a program that supports multi-threads (number of threads=10) In my case, it didn't use …
-
why 99% reads failed to align in mir-seq analysis?
written by mohammadhassanj 26Hi, After trimming the reads as discussed in below [https://www.biostars.org/p/9584040/#9584110][1] I used bowtie1 for alignment, but 99% of the reads were not aligned, **what is …
-
My rMATS output file is not showing gene symbols and only XLOC gene ID are being shown.
written by Nipan 0My --gtf file had gene_names attributes to it still no gene symbol is being shown. Am I doing something wrong? ![enter image description here][1] [1]: …
-
Error in DiffBind
written by Scabbards 0Hi, I have error said **Error in if (sum(res$peaks[[1]]$Score < 0) > 0) { : missing value where TRUE/FALSE needed In addition: There were 17 …
-
cnetplot and barplot don't show top ranked GO enrichments.
written by Shakiba 2Hi, I plotted the cnet plot with enrichResult objects. Object 1 was my filtered data with absolute log2 fold change more than 1, and object …
-
graph boxplot error
written by USER 0I would like to plot a graph like this ![enter image description here][1] but the graph is coming out like this ![enter image description here][2] …
-
How can I add text label outside the tree in iTOL ?
written by anran04100 0here is the tree in iTOL ![enter image description here][1] now I've got a txt file with information in it ![enter image description here][2] How …
Quantify long time. Can you also provide your command line? Sounds like you are using the
-toption already. If the job is running then you need to patient and wait.I let it run for 75 minutes before I stopped it
Update, ran for 12 hours and still didn't finish
Strange. Is this a NovaSeq dataset with billions of reads?
Gave up on my first sample (eight fastq files; four pairs) and tried the next sample -- finished within 1 minute! Looked through some of the fastQC reports from the first sample, nothing glaringly stood out. So not sure what's happening with that sample, especially since kallisto seems to be running on it....just not able to finish...Thanks for your input!
Files for first sample are likely not corrupt since you ran FastQC on them. Can you try just one pair and see if that completes?