Abstract
The Black Bengal goat (BBG) is a dwarf sized heritage goat (Capra hircus) breed from Bangladesh, and is well known for its high fertility, excellent meat and skin quality. Here we present the first whole genome sequence and genome-wide distributed single nucleotide polymorphisms (SNPs) of the BBG. A total of 833,469,900 raw reads consisting of 125,020,485,000 bases were obtained by sequencing one male BBG sample. The reads were aligned to the San Clemente and the Yunnan black goat genome which resulted in 98.65% (properly paired, 94.81%) and 98.50% (properly paired, 97.10%) of the reads aligning, respectively. Notably, the estimated sequencing coverages were 48.22X and 44.28X compared to published San Clemente and the Yunnan black goat genomes respectively. On the other hand, a total of 9,497,875 high quality SNPs (Q ≥ 20) along with 1,023,359 indels, and 8,746,849 high quality SNPs along with 842,706 indels were identified in BBG against the San Clemente and Yunnan black goat genomes respectively. The dataset is publicly available from NCBI BioSample (SAMN10391846), Sequence Read Archive (SRR8182317, SRR8549413 and SRR8549904), with BioProject ID PRJNA504436. These data might be useful genomic resources in conducting genome wide association studies, identification of quantitative trait loci (QTLs) and functional genomic analysis of the Black Bengal goat.
Highlights
The Black Bengal goat (BBG) is a small-sized breed of goat (Capra hircus) distributed throughout Bangladesh, West Bengal, Bihar, and Orissa regions of northeastern India
No large-scale genomic resource is available to date for this goat breed
We used the Illumina HiSeq sequencing platform to sequence the whole genome of the BBG, generated short reads and identified high quality genome wide distributed single nucleotide polymorphisms (SNPs)
Summary
The Black Bengal goat (BBG) is a small-sized breed of goat (Capra hircus) distributed throughout Bangladesh, West Bengal, Bihar, and Orissa regions of northeastern India. Keywords Black Bengal goat, whole genome sequence, short reads, SNP We used the Illumina HiSeq sequencing platform to sequence the whole genome of the BBG, generated short reads and identified high quality genome wide distributed single nucleotide polymorphisms (SNPs).
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