Understanding gene usage #1156
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Hi MiXCR developers, |
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Replies: 6 comments 1 reply
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Hi, could you please elaborate how did you produce this table? It does not look like output from MiXCR. |
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Hi @PoslavskySV, that was a table which summarize gene usage in all my samples. Here's the output from MiXCR. As you can see, there are several rows which have more than 1 V gene called. I would like to understand what are these and how to interpret these. |
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Thanks! Could you please paste exact commands you used with MiXCR? The names of the columns look quite different from the standard MiXCR output. |
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Command as below. This data is from bulk RNA-seq and MiXCR v4.3.2 was used.
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Did you rename columns manually? The column "V.name" is probably "AllVHitsWithScore" from MiXCR output. This column contain all V hits with corresponding alignment scores. E.g. the value in cell:
means that the read was aligned to two V genes: TRBV12-3 and TRBV12-4 with equal alignment score (240). You can use "bestVHit" or "bestVGene" or "bestVFamily" to have only one (best) hit in the output (see export docs). |
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I see. OK, I will try and see. |
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Did you rename columns manually? The column "V.name" is probably "AllVHitsWithScore" from MiXCR output. This column contain all V hits with corresponding alignment scores. E.g. the value in cell:
means that the read was aligned to two V genes: TRBV12-3 and TRBV12-4 with equal alignment score (240). You can use "bestVHit" or "bestVGene" or "bestVFamily" to have only one (best) hit in the output (see export docs).