Chromosome 18q deletion (18q del) syndromeis a rare genetic condition disorder, affecting approximately 1 in 40,000 to 55,000 individuals, caused…
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Newly generated, complete “end-to-end” reference genomes for the sex chromosomes of five great ape species and one lesser ape species…
Read More » Researchers from the Kops group in collaboration with researchers from the University of Edinburgh, made a surprising new discovery in…
Read More » The emergence in the Neolithic of patrilineal1 social systems, in which children are affiliated with their father’s lineage, may explain…
Read More » Published online today in Science, a new study finds that telomere lengths follow a different pattern than has thus far…
Read More » Researchers from Carnegie Mellon University’s School of Computer Science have made a significant advancement toward understanding how the human genome…
Read More » Half a century ago, scientists Jim Watson and Alexey Olovnikov independently realized that there was a problem with how our…
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