spades can run, but can't generate the configs.fastq files

[baizhantianyu]

the error information:
1:20:10.361 7857M / 15G ERROR General (hammer_tools.cpp : 194) Pair of read files "/home//genome/data/good/AS_1.raw.good.fq.gz" and "/home//genome/data/good/AS_2.raw.good.fq.gz" contain unequal amount of reads
== Error == system call for: "['/home//miniconda3/envs/spades/bin/spades-hammer', '/home//genome/spades_output/corrected/configs/config.info']" finished abnormally, OS return value: 21
the other information is ok

[baizhantianyu]

spades.log

[asl]

So, the log clearly indicates that your inputs are corrupted (and even says why).

[baizhantianyu]

So, what standard method for the unequal amount of reads of paired-end data to get the optimal assembly sequence?