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i checked both of these programs (`bbduk` and `fastp`) and it seems they use reads as inputs (fastq formats)... how can I trim my transcrip…
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He is already giving 32G, 320G for marking duplicates for exome is excessive. Is there a specific reason for using the tool?
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This looks good. Please try with using `--allow-no-sex flag`
plink --bfile your_data_phenoUP --assoc --allow-no-sex --out your_data_ph…
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SC899359_PC75420_A05 SC899359_PC75420_A05 0 0 0 2
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Please show me a few lines of phenotype updated .fam file. You can do `head
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Catalog file lists the genomes included. There seem to be 71365 unique items in field 2.
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yes sure !
![enter image description here][1]
[1]: /media/images/f0f94f6c-4387-4188-a1aa-19152a89
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Give it more memory.
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Thanks! I've already tried looking through these files, I need release 83. I am trying to find this information in the .catalog file of the…
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Possibly. You will need to know the RefSeq release version. Check in this directory: https://ftp.ncbi.nlm.nih.gov/refseq/release/release-ca…
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Hey, can you please show me a few lines of your phenotype updated .fam file? I m seeing there are 7 columns in it, that might be the proble…
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How much variance were explained by PC1 and PC2? It doesn't look like that the largest source of variation came from the genotype differenc…
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Thank you and yes, I agree going step back is the best option but I am in a hurry at the moment so I just need to stick to the transcriptom…
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Sofia
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Thank you so much for helping me out! I did the steps you mentioned but still got the same issue as shown in the snapshot 
version 2.3.6
version 2.3.6