Asset Details
Do you wish to reserve the book?
Identification of anthocyanin biosynthesis genes in rice pericarp using PCAMP
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Identification of anthocyanin biosynthesis genes in rice pericarp using PCAMP
Do you wish to request the book?
Identification of anthocyanin biosynthesis genes in rice pericarp using PCAMP
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
Identification of anthocyanin biosynthesis genes in rice pericarp using PCAMP
2019
Overview
[...]SHOREmap requires a much larger sample size; the NGM studies the genes belongs to the recessive homozygous mutant phenotype; MutMap mainly identifies the single gene‐controlled quality traits; QTL‐seq constructs only two pools showing extreme opposite trait values for a given phenotype in a segregating progeny and maps 1–2 major genes for target trait; GWAS is applicable to natural population with a large sample size and thus its cost is high, and it is also difficult to detect the rare mutations and minor effective genes. [...]we compared the SNP‐index between every two Pool‐seq to map the genomic candidate regions. For the genomic candidate regions with overlapping physical positions on the same chromosome, the intersection regions were selected as the final genomic candidate regions. [...]the regions showing a significant association with anthocyanin biosynthesis‐related genes in rice pericarp are shown in Figure c. Three genomic candidate regions were adjacent to or contained the cloned genes of anthocyanin biosynthesis (Figure c). The number of SNPs in the genomic region nearby Rd was greatly reduced (Figure e). [...]the false‐positive result may be resulted from a decrease in nucleotide polymorphism within this genomic region.
We currently cannot retrieve any items related to this title. Kindly check back at a later time.