- Krishna Lalam,
- Reddaiah Bodanapu,
- Durga Khandekar,
- Navitha Kokkonda,
- Sreehari Vasudevan,
- Navajeet Chakravartty,
- Sivarama Prasad Lekkala,
- V.B. Reddy
Authors Affiliation(s)
- AgriGenome Labs Pvt. Ltd., Hyderabad, INDIA
Can J Biotech, Volume 1, Special Issue-Supplement, Page 292, DOI: https://doi.org/10.24870/cjb.2017-a276
Presenting author: lalam.krishna@aggenome.com
Abstract
Tomato (Solanum lycopersicum) is a major crop plant and a model system for fruit development. Solanum is one of the largest angiosperm genera and includes annual and perennial plants from diverse habitats. ddRAD-seq is one of the most cost-effective methods in next generation sequencing (NGS) for generating robust genotyping data which permits high throughput simultaneous discovery and genotyping of sequence polymorphism either with or without an existing reference genome. Advantage of ddRAD technique was investigated by performing data analysis of sequence obtained through low pass whole genome sequencing and ddRAD protocol. Here we present a high-quality reduced represented genome sequence of domesticated tomato with the aim of understanding genetic variations in cultivated tomato; single nucleotide polymorphism (SNP) markers covering the whole genome of eight cultivars and four F1 hybrids were developed through Genotyping-By-Sequencing. We have sequenced twelve tomato varieties using Illumina HiSeq 4000, next generation sequencing platform. The raw data was subjected to preprocessing and aligned with reference tomato genome downloaded from ensembl release 36. The SNPs/INDELs were identified for each of the tomato varieties. A total of 30746 SNPs and 913 INDELs were identified. We investigated for homozygous polymorphic markers between PKM-1 and Arka Abha and found 745 markers which can be used as markers for fingerprinting.The homozygous polymorphic markers will be utilized for genetic mapping and trait association in a mapping population.