老师您好，请问在论文返修中审稿人问：（1）非编码RNA鉴定的具体功能是什么？What’s the detailed function for the non-coding RNA identification?我在论文中写了有多少个各类的ncrna。请问还需要补充什么呀。（2）该组装高度碎片化，连续序列N50仅为2兆碱基——远低于T2T基因组时代的预期标准。这很可能由于HiFi数据不足（仅约40吉碱基）所致；我们预计≥80吉碱基的HiFi测序读数将显著提升连续性。此外，鉴于该物种的极端杂合性，采用ONT长读长可能获得更优的组装结果。The assembly is highly fragmented, with a contig N50 of only 2 Mb—far below the standard expected in the era of T2T genomes. This is most likely due to insufficient HiFi data (only ~40 Gb); we anticipate that ≥80 Gb of HiFi reads would substantially improve contiguity. Moreover, given the extremely high heterozygosity of this species, using ONT long reads may yield a better assembly. 我的虫子比较小，且是单一源头的克隆群，DNA量不够，只测了30G的hifi，没办法补数据了应该怎么回复。（3）survey结果是0.97G，组装结果是1.15G。杂合1.19。请问怎么回答好一点