Open KS751515 opened 1 year ago
Hi @KS751515,
It appears that you have quantified the genome (i.e. you have computed an abundance for each chromosome) rather than the transcriptome (i.e. an abundance for each gene transcript). The reference should be the reference transcriptome rather than the reference genome (depending on the specific annotation, this should have on the order of ~150,000-200,000 reference sequences.
Best, Rob
I am completely new to Bioinfomatic. I started with Galaxy since it require no coding. When execute Salmon, I found the result is very strange.
195 lines format tabular database ?
the length are huge.
Name Length EffectiveLength TPM NumReads 1 248956422 248956245.175 454.257509 2624930.608 10 133797422 133797245.175 273.316948 848802.051 11 135086622 135086445.175 488.035486 1530227.002 12 133275309 133275132.175 506.506671 1566848.399 13 114364328 114364151.175 146.273092 388281.806 14 107043718 107043541.175 349.454058 868246.901 15 101991189 101991012.175 450.603218 1066716.167 16 90338345 90338168.175 396.208587 830783.477 17 83257441 83257264.175 627.875560 1213356.444 18 80373285 80373108.175 134.057567 250089.112 19 58617616 58617439.175 889.185152 1209794.846 2 242193529 242193352.175 386.373763 2172013.559 20 64444167 64443990.175 400.290070 598756.066 21 46709983 46709806.175 321.808746 348898.092 22 50818468 50818291.175 428.166522 505039.621 3 198295559 198295382.175 253.622671 1167329.228 4 190214555 190214378.175 176.536396 779417.738 5 181538259 181538082.175 276.829027 1166465.921 6 170805979 170805802.175 436.693266 1731297.895 7 159345973 159345796.175 293.251440 1084609.614 8 145138636 145138459.175 346.904465 1168651.671 9 138394717 138394540.175 292.533191 939694.730 MT 16569 16392.175 925959.459914 352306.967 X 156040895 156040718.175 182.793129 662049.550 Y 57227415 57227238.175 2.760039 3666.154 KI270728.1 1872759 1872582.175 0.059275 2.576 KI270727.1 448248 448071.175 3.830303 39.836 KI270442.1 392061 391884.175 2.210647 20.108 KI270729.1 280839 280662.175 2.358259 15.363 GL000225.1 211173 210996.175 6.939465 33.985 KI270743.1 210658 210481.175 1.953268 9.543 GL000008.2 209709 209532.175 8.374637 40.730 GL000009.2 201709 201532.175 7.102359 33.223 KI270747.1 198735 198558.175 0.000000 0.000 KI270722.1 194050 193873.175 0.000000 0.000 GL000194.1 191469 191292.175 235.664877 1046.369 KI270742.1 186739 186562.175 16.393393 70.988 GL000205.2 185591 185414.175 75.780709 326.133 GL000195.1 182896 182719.175 121.039913 513.340 KI270736.1 181920 181743.175 0.000000 0.000 KI270733.1 179772 179595.175 30992.190385 129193.190 GL000224.1 179693 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I use Transcripts FASTA file | 304 : Primary assembly uncompressed
GTF also from ensemble!
the rest I only use default.
Does any body know what could be wrong?
Thank you so much in advance.
KS