Library construction was performed at N2Jenomics Lab Pvt. Ltd., New Delhi, India. All eight samples (Sample IDs: 786, 788, 795, 796, 797, 798, 799, and 801) passed the quality control criteria and were approved for sequencing. Whole-genome sequencing was carried out on the Illumina platform using paired-end chemistry with an average read length of 150 bp. Each library was sequenced to produce approximately 30–35  Gb of clean data per sample, achieving an average coverage of around 10× across the genome. The GC content among samples ranged from 42.7% to 43.5%. The base quality metrics showed that more than 98% of bases had Q20 and more than 94% had Q30 scores, indicating high data quality. For all samples, the mean quality score was above Q36, and over 94% of bases exceeded the Q30 threshold. Data yield per sample ranged from 30–35 GB, ensuring sufficient depth for downstream genome-wide analyses.