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We also mapped an additional nine events solely by SNP arrays.
We mapped an additional 80 BACs, extending the set to 125 markers on macrochromosomes and 42 on microchromosomes.
We have also mapped an additional six BES microsatellites onto linkage groups of the INRA genetic map (Additional file 1, sheet 1).
From the initial parental maps of the C14×C15 mapping population described by de Miguel et al. (2012), we mapped an additional set of 980 SNPs from the 12k SNP-array described by Chancerel et al. (2011) and 273 SNPs from a 1,536 SNP-array (Sáez-Laguna et al. unpublished) here to increase the number of anchor markers common to other maps.
We identified 196 regulated conserved phosphorylation sites between human and rat in their insulin stimulated phosphoproteomes, of which 83 were already known and annotated in PhosphoSitePlus, hence, we mapped an additional 113 novel sites which is an increase of 136 % in mapping coverage compared to those retrieved from PhosphoSitePlus [ 4] alone.
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Using this genetic/physical synteny, we have also been able to electronically map an additional 20,000 common bean EST contigs and singletons relative to soybean.
If the corresponding marker was linked to a region with a MTRD≥70%, it would mean that we had been very unfortunate in not having mapped any additional markers with a MTRD between 61% and 70%.
In the existence and uniqueness proofs of fixed points of α-admissible maps, an additional property is required.
Further mapping an additional 55 offspring places male sterility in a gene-dense, 338-kb region of chromosome 4.
To complete the physical map, an additional whole genome BAC library was developed from Hope, and screened with markers flanking the gaps.
In each case, we were able to map an additional approximately four million reads (~6.5% of the original set of sequenced reads).
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