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Finally, by using a small number of insertion/deletion (indel) markers, each of which is specific to a recombination block, we identified a putative locus for soybean hilum color with minimal screening.
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Using primary human CD4+ T cells, and by blocking STAT6 with RNAi, we identified a number of direct and indirect targets of STAT6 with ChIP sequencing.
Based on haplotype blocks, we identified clear breakpoints for all Est-like regions (Table 4).
We identified a haplotype block of eight SNPs including rs9310784.
In our systematic analysis of hematopoiesis in Mysm1−/− mice, we identified a first block at the stage of HSCs and the transition to LMPPs.
As summarized in Table 2 and detailed in Additional file 4, we identified a total of 124 putative functional SNPs in 70 of the haplotype blocks identified herein.
By comparing the location of these blocks among the three genomes, it is clear that numerous blocks that we identified in one pairwise analysis were found to completely or partially overlap blocks identified in other pairwise analyses, indicating that a substantial number of blocks of synteny may be conserved among the three species.
Prior to development of T-ALL in our TLX1 mice, we also identified a partial block in T-cell differentiation.
The front-end of SDR is the signal detection block which identifies a signal transmission [6].
Therefore the phosphorylation of p53 should be blocked when we identify bistability.
In each of the s blocks, we then identify whether a break occurred in the variable species using the criteria defined above.
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