Genetic basis for congenital heart disease: revisited: a scientific statement from the American Heart Association

ME Pierpont, M Brueckner, WK Chung, V Garg… - Circulation, 2018 - Am Heart Assoc
This review provides an updated summary of the state of our knowledge of the genetic
contributions to the pathogenesis of congenital heart disease. Since 2007, when the initial …

Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences

C Manzoni, DA Kia, J Vandrovcova… - Briefings in …, 2018 - academic.oup.com
Advances in the technologies and informatics used to generate and process large biological
data sets (omics data) are promoting a critical shift in the study of biomedical sciences. While …

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

C Turnbull, RH Scott, E Thomas, L Jones… - Bmj, 2018 - bmj.com
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS Page 1 The
100 000 Genomes Project: bringing whole genome sequencing to the NHS In partnership with …

The Sorghum bicolor reference genome: improved assembly, gene annotations, a transcriptome atlas, and signatures of genome organization

RF McCormick, SK Truong, A Sreedasyam… - The Plant …, 2018 - Wiley Online Library
Sorghum bicolor is a drought tolerant C4 grass used for the production of grain, forage,
sugar, and lignocellulosic biomass and a genetic model for C4 grasses due to its relatively …

CHESS: a new human gene catalog curated from thousands of large-scale RNA sequencing experiments reveals extensive transcriptional noise

M Pertea, A Shumate, G Pertea, A Varabyou… - Genome biology, 2018 - Springer
We assembled the sequences from deep RNA sequencing experiments by the Genotype-
Tissue Expression (GTEx) project, to create a new catalog of human genes and transcripts …

Open questions: How many genes do we have?

SL Salzberg - BMC biology, 2018 - Springer
Open questions: How many genes do we have? | BMC Biology Skip to main content
SpringerLink Account Menu Find a journal Publish with us Track your research Search Cart …

Variant ribosomal RNA alleles are conserved and exhibit tissue-specific expression

MM Parks, CM Kurylo, RA Dass, L Bojmar, D Lyden… - Science …, 2018 - science.org
The ribosome, the integration point for protein synthesis in the cell, is conventionally
considered a homogeneous molecular assembly that only passively contributes to gene …

[HTML][HTML] Fluorescence in situ hybridization (FISH): History, limitations and what to expect from micro-scale FISH?

D Huber, LV Von Voithenberg, GV Kaigala - Micro and Nano Engineering, 2018 - Elsevier
In this article, we review an important cytogenetic technique-fluorescence in situ
hybridization (FISH)-which is used for obtaining spatial genomic and transcriptomic …

LncRNA SNHG7 sponges miR-216b to promote proliferation and liver metastasis of colorectal cancer through upregulating GALNT1

Y Shan, J Ma, Y Pan, J Hu, B Liu, L Jia - Cell death & disease, 2018 - nature.com
Accumulating evidence suggests long noncoding RNAs (lncRNAs) play an important role in
cancer progression. However, the function of lncRNA SNHG7 in colorectal cancer (CRC) …

A fast adaptive algorithm for computing whole-genome homology maps

C Jain, S Koren, A Dilthey, AM Phillippy, S Aluru - Bioinformatics, 2018 - academic.oup.com
Motivation Whole-genome alignment is an important problem in genomics for comparing
different species, mapping draft assemblies to reference genomes and identifying repeats …