scholarly journals Novel Exons and Splice Variants in the Human Antibody Heavy Chain Identified by Single Cell and Single Molecule Sequencing

PLoS ONE ◽  
2015 ◽  
Vol 10 (1) ◽  
pp. e0117050 ◽  
Author(s):  
Christopher Vollmers ◽  
Lolita Penland ◽  
Jad N. Kanbar ◽  
Stephen R. Quake
2020 ◽  
Vol 11 ◽  
Author(s):  
Catherine Tang ◽  
Davide Bagnara ◽  
Nicholas Chiorazzi ◽  
Matthew D. Scharff ◽  
Thomas MacCarthy

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Moriah Gidoni ◽  
Omri Snir ◽  
Ayelet Peres ◽  
Pazit Polak ◽  
Ida Lindeman ◽  
...  

mSystems ◽  
2021 ◽  
Vol 6 (2) ◽  
Author(s):  
Mengqi Sun ◽  
Yuanchao Zhan ◽  
David Marsan ◽  
David Páez-Espino ◽  
Lanlan Cai ◽  
...  

ABSTRACT Viruses are ubiquitous and abundant in the oceans, and viral metagenomes (viromes) have been investigated extensively via several large-scale ocean sequencing projects. However, there have not been any systematic viromic studies in estuaries. Here, we investigated the viromes of the Delaware Bay and Chesapeake Bay, two Mid-Atlantic estuaries. Deep sequencing generated a total of 48,190 assembled viral sequences (>5 kb) and 26,487 viral populations (9,204 virus clusters and 17,845 singletons), including 319 circular viral contigs between 7.5 kb and 161.8 kb. Unknown viruses represented the vast majority of the dominant populations, while the composition of known viruses, such as pelagiphage and cyanophage, appeared to be relatively consistent across a wide range of salinity gradients and in different seasons. A difference between estuarine and ocean viromes was reflected by the proportions of Myoviridae, Podoviridae, Siphoviridae, Phycodnaviridae, and a few well-studied virus representatives. The difference in viral community between the Delaware Bay and Chesapeake Bay is significantly more pronounced than the difference caused by temperature or salinity, indicating strong local profiles caused by the unique ecology of each estuary. Interestingly, a viral contig similar to phages infecting Acinetobacter baumannii (“Iraqibacter”) was found to be highly abundant in the Delaware Bay but not in the Chesapeake Bay, the source of which is yet to be identified. Highly abundant viruses in both estuaries have close hits to viral sequences derived from the marine single-cell genomes or long-read single-molecule sequencing, suggesting that important viruses are still waiting to be discovered in the estuarine environment. IMPORTANCE This is the first systematic study about spatial and temporal variation of virioplankton communities in estuaries using deep metagenomics sequencing. It is among the highest-quality viromic data sets to date, showing remarkably consistent sequencing depth and quality across samples. Our results indicate that there exists a large pool of abundant and diverse viruses in estuaries that have not yet been cultivated, their genomes only available thanks to single-cell genomics or single-molecule sequencing, demonstrating the importance of these methods for viral discovery. The spatiotemporal pattern of these abundant uncultivated viruses is more variable than that of cultured viruses. Despite strong environmental gradients, season and location had surprisingly little impact on the viral community within an estuary, but we saw a significant distinction between the two estuaries and also between estuarine and open ocean viromes.


mAbs ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 1778435 ◽  
Author(s):  
Zehua Sun ◽  
Chuan Chen ◽  
Wei Li ◽  
David R. Martinez ◽  
Aleksandra Drelich ◽  
...  

2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Jayoung Ku ◽  
Ryul Kim ◽  
Dongchan Kim ◽  
Daeyoon Kim ◽  
Seulki Song ◽  
...  

Abstract Aminoacyl-tRNA synthetase-interacting multifunctional protein 2 (AIMP2) is a non-enzymatic component required for the multi-tRNA synthetase complex. While exon 2 skipping alternatively spliced variant of AIMP2 (AIMP2-DX2) compromises AIMP2 activity and is associated with carcinogenesis, its clinical potential awaits further validation. Here, we found that AIMP2-DX2/AIMP2 expression ratio is strongly correlated with major cancer signaling pathways and poor prognosis, particularly in acute myeloid leukemia (AML). Analysis of a clinical patient cohort revealed that AIMP2-DX2 positive AML patients show decreased overall survival and progression-free survival. We also developed targeted RNA-sequencing and single-molecule RNA-FISH tools to quantitatively analyze AIMP2-DX2/AIMP2 ratios at the single-cell level. By subclassifying hematologic cancer cells based on their AIMP2-DX2/AIMP2 ratios, we found that downregulating AIMP2-DX2 sensitizes cells to anticancer drugs only for a subgroup of cells while it has adverse effects on others. Collectively, our study establishes AIMP2-DX2 as a potential biomarker and a therapeutic target for hematologic cancer.


2018 ◽  
Vol 37 (18) ◽  
Author(s):  
Ying‐Cing Lin ◽  
Simone Pecetta ◽  
Jon M Steichen ◽  
Sven Kratochvil ◽  
Eleonora Melzi ◽  
...  

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