scholarly journals A computational framework for converting high-throughput DNA sequencing data into neural circuit connectivity

2018 ◽  
Author(s):  
Hassana Oyibo ◽  
Cang Cao ◽  
Daniel D. Ferrante ◽  
Huiqing Zhan ◽  
Alex Koulakov ◽  
...  

There is growing interest in determining the connectivity of neural circuits—the “connectome”—at single neuron resolution. Most approaches to circuit mapping rely on either microscopy or physiology, but these approaches have very limited throughput. We have recently proposed BOINC (Barcoding of Individual Neuronal Connectivity), a radically different approach to connectivity mapping based on high-throughput DNA sequencing. Here we describe the set of computational algorithms that serve to convert sequencing data into neural connectivity. We apply our computational pipeline to the results of proof-of-principle experiments illustrating an implementation of BOINC based on pseudorabies virus (PRV). PRV is capable of traversing individual synapses and carry DNA barcodes from one cell to another. Using this high-throughput sequencing data, we obtain 456-by-486 connectivity matrix between putative neurons. An inexpensive high-throughput technique for establishing circuit connectivity at single neuron resolution would represent a major advance in neuroscience.

2011 ◽  
Vol 21 (5) ◽  
pp. 734-740 ◽  
Author(s):  
M. Hsi-Yang Fritz ◽  
R. Leinonen ◽  
G. Cochrane ◽  
E. Birney

2018 ◽  
Author(s):  
Curtis J Layton ◽  
Peter L McMahon ◽  
William J Greenleaf

SummaryHigh-throughput DNA sequencing techniques have enabled diverse approaches for linking DNA sequence to biochemical function. In contrast, assays of protein function have substantial limitations in terms of throughput, automation, and widespread availability. We have adapted an Illumina high-throughput sequencing chip to display an immense diversity of ribosomally-translated proteins and peptides, and then carried out fluorescence-based functional assays directly on this flow cell, demonstrating that a single, widely-available high-throughput platform can perform both sequencing-by-synthesis and protein assays. We quantified the binding of the M2 anti-FLAG antibody to a library of 1.3×104 variant FLAG peptides, exploring non-additive effects of combinations of mutations and discovering a “superFLAG” epitope variant. We also measured the enzymatic activity of 1.56×105 molecular variants of full-length of human O6-alkylguanine-DNA alkyltransferase (SNAP-tag). This comprehensive corpus of catalytic rates linked to amino acid sequence perturbations revealed amino acid interaction networks and cooperativity, linked positive cooperativity to structural proximity, and revealed ubiquitous positively-cooperative interactions with histidine residues.


2017 ◽  
Author(s):  
Yuchao Jiang ◽  
Rujin Wang ◽  
Eugene Urrutia ◽  
Ioannis N. Anastopoulos ◽  
Katherine L. Nathanson ◽  
...  

AbstractHigh-throughput DNA sequencing enables detection of copy number variations (CNVs) on the genome-wide scale with finer resolution compared to array-based methods, but suffers from biases and artifacts that lead to false discoveries and low sensitivity. We describe CODEX2, a statistical framework for full-spectrum CNV profiling that is sensitive for variants with both common and rare population frequencies and that is applicable to study designs with and without negative control samples. We demonstrate and evaluate CODEX2 on whole-exome and targeted sequencing data, where biases are the most prominent. CODEX2 outperforms existing methods and, in particular, significantly improves sensitivity for common CNVs.


2013 ◽  
Vol 30 (4) ◽  
pp. 409-415
Author(s):  
Zexuan Zhu ◽  
Yongpeng Zhang ◽  
Zhuhong You ◽  
Liang Jiang ◽  
Zhen Ji

PLoS ONE ◽  
2016 ◽  
Vol 11 (5) ◽  
pp. e0155461 ◽  
Author(s):  
José M. Abuín ◽  
Juan C. Pichel ◽  
Tomás F. Pena ◽  
Jorge Amigo

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