Hi every one,
We sent 100 cases and 100 controls samples to the sequencing company for exon sequencing data, we are afraid that the company might make mistakes when they sent the data back. If one sample is belong to the case group and the company misidentified it and sent us the data as a control sample, we will get wrong results. So we want to know if there are some methods to mark a sample before building library and we can identify each sample from the sequecing data?
Thanks.
We sent 100 cases and 100 controls samples to the sequencing company for exon sequencing data, we are afraid that the company might make mistakes when they sent the data back. If one sample is belong to the case group and the company misidentified it and sent us the data as a control sample, we will get wrong results. So we want to know if there are some methods to mark a sample before building library and we can identify each sample from the sequecing data?
Thanks.
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