Open l1y1y opened 4 months ago
Yes, you can run scTE with bulk RNA-seq data, but need to set with the option-CB False -UMI False --hdf5 False
Yes, you can run scTE with bulk RNA-seq data, but need to set with the option
-CB False -UMI False --hdf5 False
Thank you, thank you for your answer
Yes, you can run scTE with bulk RNA-seq data, but need to set with the option
-CB False -UMI False --hdf5 False
@jphe hello, I ran the program, used RNA-seq data, added annotation files, and set CB False -UMI False --hdf5 False, but my results seemed weird. Can you help me check the results? Is it correct? Thanks barcodes,(CATTC)n,0610005C13Rik,0610006L08Rik,0610009B22Rik,0610009E02Rik,0610009L18Rik,0610010F05Rik,0610010K14Rik,0610012D04Rik,0610012G03Rik,0610025J13Rik, AC125544.1,AC126027.1,AC126029.1,AC126029.2,AC126031.1,AC126031.2,AC126031.3,AC126031.4,AC126040.1,AC126040.2,AC126041.1,AC126046.1,AC126254.1, ,Adgre1,Adgre4,Adgre5,Adgrf1,Adgrf2,Adgrf3,Adgrf4,Adgrf5,Adgrg1,Adgrg2,Adgrg3,Adgrg4,Adgrg5,Adgrg6,Adgrg7,Adgrl1,Adgrl2,Adgrl3,Adgrl4,Adgrv1,Adh1,Adh4,Adh5,Adh6-ps1,Adh6a,Adh6b,Adh7 Gm11472,Gm11473,Gm11474,Gm11475,Gm11476,Gm11478,Gm11479,Gm11480,Gm11481,Gm11482,Gm11483,Gm11484,Gm11485,Gm11486, Olfr844,Olfr845,Olfr846,Olfr847,Olfr848-ps1,Olfr849,Olfr850,Olfr851,Olfr852-ps1,Olfr853,Olfr854,Olfr855,Olfr856-ps1,Olfr857,Olfr858-ps1,Olfr859,Olfr860,Olfr861-ps1,Olfr862,Olfr863-ps1, ,0,1,74,1040,21,54,1,20,157,36,5,15,6,0,1110,63,2,1422,73,38,0,679,68,208,3,1,33,13,2,2,21,0,0,24,349,587,14,26,235,312,17,2,0,5,4,0,6,12,31,270,75,36,690,16,713,162,990,5,0,10,19,174,251,0,12,0,2 A csv document was generated with only these contents. After I read it, there were two rows and more than 50,000 columns. I would like to ask, should I process this result? I added an annotation file. Shouldn’t the output result be the name of the gene?
It's correct, the column name is gene name
It's correct, the column name is gene name
OK, thank you and wish you good luck in your research
Thank you very much for your help, thank you
I want to know if this tool can handle RNA-seq data, or can it only handle single-cell data?
I wish you good luck with your research