Sentence examples for mapping in chickpea from inspiring English sources

Limited genomic resources and low levels of genetic variability in the primary gene pool, however, have restricted the practical application of genetic mapping in chickpea [ 8].

We, therefore, selected this ABI3VP1 TF gene localized at the major and robust SW-governing QTL interval (qSW4.2) as target candidate for understanding its significance in seed weight regulation through high-resolution gene haplotype-specific association/LD mapping in chickpea.

Very recently, Hiremath et al. developed KASpar assays for 2005 SNPs in chickpea and used these for genetic diversity analysis and genetic mapping in chickpea and comparative mapping in legumes.

The latest draft genome sequences of desi and kabuli chickpea cultivars enabled to select a large number of genome-wide SSR and SNP markers from pseudomolecules of eight chromosomes based on their physical positions (bp) for uniform as well as high saturation genome and gene/QTL mapping in chickpea.

The large-scale genotyping information of these markers in RILs was correlated/integrated with their replicated multi-location field phenotyping data to identify the novel genomic regions harbouring the major and robust QTLs associated with four agro-morphological traits through genetic/QTL mapping in chickpea.

It is worthwhile to mention that a high robust amplification efficiency (96.5%) and high intra-specific polymorphic potential (34%) has been recently been exploited for the genotyping and trait association mapping in Chickpea using the 1108 transcription factor gene-derived microsatellite (TFGMS) and 161 transcription factor functional domain-associated microsatellite (TFFDMS) markers (69).

Discrepancies in genome size of chickpea was also reported in an earlier study of the development of physical map in chickpea; however, they reported more genome size than the expected 738 Mb (Zhang et al. 2010).

Further, owing to their ability of interspecific transferability, STMS markers have been reported to be the most elite anchor markers for merging different genetic maps and for setting up a high genome coverage consensus map in chickpea [ 13, 20].

Similarly, another set of 46,270 BAC-end sequences for CAH1 library that were used to develop novel SSR markers and development of high-density genetic map in chickpea were also used for in silico mapping onto draft chickpea genome during the present study.

A set of 839 including 470 genic and genomic SSR markers (Supplementary Fig. S2) and 369 TF gene-derived SNP markers (Supplementary Fig. S3) showing polymorphism between parental accessions were genotyped in 229 individuals of a RIL mapping population (ICC 4958 × ICC 17160) to construct an inter-specific genetic linkage map in chickpea.

A high-density inter-specific genetic linkage map constructed by high-throughput genotyping of genome-wide 834 genic and genomic SSR and SNP markers in our study would expedite genome mapping and targeted mapping of genes/QTLs associated with traits of agricultural importance in chickpea, including comparative mapping across legumes.