✦ LIBER ✦

Correction: Closing gaps in the human genome using sequencing by synthesis

✍ Scribed by Manuel Garber, Michael C Zody, Harindra C Arachchi, Aaron Berlin…

Book ID: 120702017
Publisher: BioMed Central
Year: 2011
Tongue: English
Weight: 232 KB
Volume: 12
Category: Article
ISSN: 1465-6906
DOI: 10.1186/gb-2011-12-4-403

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Closing gaps in the human genome using s

Closing gaps in the human genome using sequencing by synthesis

✍ Manuel Garber, Michael C Zody, Harindra M Arachchi, Aaron Berlin… 📂 Article 📅 2009 🏛 BioMed Central 🌐 English ⚖ 198 KB

Closing gaps in the human genome with fo

Closing gaps in the human genome with fosmid resources generated from multiple individuals

✍ Bovee, Donald; Zhou, Yang; Haugen, Eric; Wu, Zaining; Hayden, Hillary S; Gillett 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 351 KB

An assessment of the sequence gaps: Unfi

An assessment of the sequence gaps: Unfinished business in a finished human genome

✍ Eichler, Evan E.; Clark, Royden A.; She, Xinwei 📂 Article 📅 2004 🏛 Nature Publishing Group 🌐 English ⚖ 225 KB

Conversion of AFLP markers to sequence-s

Conversion of AFLP markers to sequence-specific markers for closely related lines in rice by use of the rice genome sequence

✍ Kenta Shirasawa; Sachie Kishitani; Takeshi Nishio 📂 Article 📅 2004 🏛 Springer Netherlands 🌐 English ⚖ 133 KB

Systematic analysis of transcribed loci

Systematic analysis of transcribed loci in ENCODE regions using RACE sequencing reveals extensive transcription in the human genome

✍ Jia Qian Wu, Jiang Du, Joel Rozowsky, Zhengdong Zhang, Alexander E Urban… 📂 Article 📅 2008 🏛 BioMed Central 🌐 English ⚖ 441 KB

Genomic sequence correction by single-st

Genomic sequence correction by single-stranded DNA oligonucleotides: role of DNA synthesis and chemical modifications of the oligonucleotide ends

✍ Petter Angell Olsen; Markus Randøl; Luisa Luna; Tom Brown; Stefan Krauss 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 344 KB

## Abstract ## Background Single‐stranded oligonucleotides (ssODN) can induce site‐specific genetic alterations in selected mammalian cells, but the involved mechanisms are not known. ## Methods We corroborate the potential of genomic sequence correction by ssODN using chromosomally integrated m