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More alerting is the high "host-cell contamination" of this experiment, which leaves not much more than 1 million reads left that map to the bacterial genome. Authors should provide additional efforts to assure that this low number of reads is still sufficient for comparative gene expression studies, even when using a rather traditional cutoff of >= 10 RPKM. Furthermore, the differences in effective sequencing depth between the growth conditions HeLa and DMEM seem to reach up to ~20fold. Either statistics or visual inspection of the predicted DE genes (e.g., in the ranking of all genes) should be presented. The problem of E.coli concentration in HeLa experiments should at least be mentioned, or better discussed, in the main manuscript. ´ó¼Ò°ïæ¿´¿´£¬±êעΪºÚÌåµÄÕâ¾ä»°Either statistics or visual inspection of the predicted DE genes (e.g., in the ranking of all genes) should be presented.¸ÃÔõô»Ø´ð¡£»òÕßÎÒÃǸÃ×öЩʲô |
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yangbin1
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