Linked-Reads: Find the Answer to What's Been Missing
Learn more about assembling the genome easily with this poster from The Scientist and 10X Genomics!
The Scientist Creative Services Team
Sep 30, 2017
Organisms and biology are immensely complex, and to truly understand disease mechanisms, heritability, potential diagnoses, and development of therapies, we need access to more genomic information. Linked-Reads constructs long-range information from short-reads to provide access to hidden and inaccessible information. With Linked-Reads, researchers now have the power to resolve ambiguous single nucleotide variants, provide phasing and haplotype information, identify structural variants, and assemble genomes without the need for a reference sequence.
Download this poster from The Scientist, sponsored by 10X Genomics to learn about linked reads, structural variants, and resolving haplotypes!
Interested in reading more?
The Scientist ARCHIVES
Become a Member of
Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!