Hi Finally at the point of doing some differential expression analysis
I used HTseq2 to align my data to mm10. That was successful. I used the " Back to Unnamed history htseq-count on collection 316" file and the corresponding mate file i.e treated group. In both cases when I fed the data into DEseq2 or EdgeR I get error. The file is highlighted in red. In the case of EdgeR I get the following Error
Fatal error: Exit code 1 ()
Error in `row.names<-.data.frame`(`*tmp*`, value = c("X0", "X0", "X0", :
duplicate 'row.names' are not allowed
Calls: row.names<- -> row.names<-.data.frame
Warning message:
non-unique value when setting 'row.names': ‘X0’
Here are the first couple lines from of text output from the HTseq feature file for one of the replicates
00R_AC107638.2 0
00R_Pgap2 0
0610009O20Rik 1020
1110020A21Rik 18
1110036E04Rik 0
1600014C23Rik 3
1600017P15Rik 0
1700015F17Rik 1
1700018M17Rik 0
1700022N22Rik 4
1700024J04Rik 0
1700028P14Rik 0
1700037F24Rik 0
1700067P10Rik 0
1700086O06Rik 60
1700123K08Rik 0
1810049J17Rik 3
1810055G02Rik 1051
19.47525802-47711187.1 0
2.145048962-146444327.1 0
2010001E11Rik 0
2010003K11Rik 1
2010015M23Rik 4
2010110K18Rik 14
2010300F17Rik 82
2210008F06Rik 14
2310026I22Rik 0
2310031A07Rik 2
2310039H08Rik 254
2410015M20Rik 1081
2410024N13Rik 0
2610020F03Rik 0
2700012I20Rik 4
2700016F22Rik 3
2700046G09Rik 16
2700062C07Rik 273
2810403A07Rik 1320
2810425M01Rik 1
2900055J20Rik 0
3100002H09Rik 0
3110018I06Rik 0
3110021N24Rik 3
3110070M22Rik 1
3110082I17Rik 271
4732491K20Rik 41
4831440E17Rik 2
4833407H14Rik 0
4833418N17Rik 0
4921501E09Rik 0
4921524L21Rik 0
4930426L09Rik 4
4930442H23Rik 1
4930444M15Rik 1
4930445N18Rik 3
4930455D15Rik 1
4930465K10Rik 1
4930480K23Rik 19
4930505N22Rik 1
4930507D05Rik 4
4930515G13Rik 0
4930518I15Rik 0
4930519P11Rik 0
4930524J08Rik 16
4930535I16Rik 0
4930546C10Rik 0
4930552P12Rik 3
4930553M12Rik 0
4930563E18Rik 0
4930583I09Rik 0
4930598A11Rik 0
4931403G20Rik 0
4931409K22Rik 1
4931440J10Rik 1
4932430I15Rik 0
4933412A08Rik 0
4933415A04Rik 0
4933427I04Rik 0
5031415H12Rik 9
5330417H12Rik 0
5730596B20Rik 0
5930422O12Rik 0
6030445D17Rik 23
6030452D12Rik 0
6330403N20Rik 0
6530411M01Rik 0
8030462N17Rik 603
9.104944562-105295281.1 0
9030612E09Rik 53
9130008F23Rik 36
9130011E15Rik 733
9130213A22Rik 10
930412E21Rik 0
9330132A10Rik 0
9330136K24Rik 5
9330161L09Rik 6
9430025C20Rik 1
9430097D07Rik 1
9430098F02Rik 0
9530027J09Rik 2
9830107B12Rik 0
9930104L06Rik 97
9930111J21Rik1 71
9930111J21Rik2 329
A130006I12Rik 4
A1bg 0
A1cf 0
A230072I06Rik 0
A2m 0
A330032B11Rik 0
A330069E16Rik 19
A330094K24Rik 0
A3galt2 4
A430046D13Rik 79
A4galt 968
A4gnt 2
A530064D06Rik 0
A530084C06Rik 14
A630075F10Rik 0
A730015C16Rik 1
A730061H03Rik 0
A730071L15Rik 1
A830052D11Rik 2
A930002H24Rik 14
A930007I19Rik 10
A930024N18Rik 0
A930035D04Rik 27
AA543186 13
AC012382.1 2
AC012382.2 0
AC015800.4 44
AC021667.1 0
AC025622.3 2
AC026231.3 1
AC026478.1 12764
AC027285.1 0
AC034099.1 0
AC068006.3 0
AC068006.4 0
Is there a formatting issue? Is there someway to curate the data prior to piping into DESeq2/EdgeR
Mike