reproducible analysis
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2021 ◽  
Author(s):  
Douglas F Porter ◽  
Raghav M Garg ◽  
Robin M Meyers ◽  
Weili Miao ◽  
Luca Ducoli ◽  
...  

The easyCLIP protocol describes a method for both normal CLIP library construction and the absolute quantification of RNA cross-linking rates, data which could be usefully combined to analyze RNA-protein interactions. Using these cross-linking metrics, significant interactions could be defined relative to a set of random non-RBPs. The original easyCLIP protocol did not use index reads, required custom sequencing primers, and did not have an easily reproducible analysis workflow. This short paper attempts to amend these deficiencies. It also includes some additional technical experiments and investigates the usage of alternative adapters. The results here are intended to allow more options to easily perform and analyze easyCLIP.


2021 ◽  
Author(s):  
Simone Picelli ◽  
Vincent Hahaut

The single-cell RNA-sequencing (scRNA-seq) field has evolved tremendously since the first paper was published back in 2009. While the first methods analysed just a handful of cells, the throughput and performance rapidly increased over a very short timespan. However, it was not until the introduction of emulsion droplets methods, that the robust and reproducible analysis of thousands of cells became feasible. Despite generating data at a speed and a cost per cell that remains unmatched by full-length protocols like Smart-seq, scRNA-seq in droplets still comes with the drawback of addressing only the terminal portion of the transcripts, thus lacking the required sensitivity for comprehensively analyzing the transcriptome of individual cells. Building upon the existing Smart-seq2/3 workflows, we developed FLASH-seq (FS), a new full-length scRNA-seq method capable of detecting a significantly higher number of genes than both previous versions, requiring limited hands-on time and with a great potential for customization.


2021 ◽  
Author(s):  
Beckey DeLucia ◽  
Sergey Samorezov ◽  
Megan T Zangara ◽  
Rachel L Markley ◽  
Lucas J Osborn ◽  
...  

AbstractAccurate and reproducible analysis of mouse small and large intestinal lumen is key for research involving intestinal pathology in preclinical models. Currently, there is no easily accessible, standardized method that allows researchers of different skill levels to consistently dissect intestines in a time-efficient manner. Here, we describe the design and use of the 3D printed “Mouse Intestinal Slicing Tool” (MIST), which can be used to longitudinally prepare murine intestines for further analysis. We benchmarked the MIST against a commonly used procedure involving scissors to make a longitudinal cut along the intestines. Use of the MIST halved the time per mouse to prepare the intestines and outperformed alternative methods in smoothness of the cutting edge and general reproducibility. By sharing the plans for printing the MIST, we hope to contribute a uniformly applicable method for saving time and increasing consistency in studies of the mouse gastrointestinal tract.


2021 ◽  
Author(s):  
Jennifer R Eng ◽  
Elmar Bucher ◽  
Zhi Hu ◽  
Ting Zheng ◽  
Summer Gibbs ◽  
...  

Multiplex imaging technologies are increasingly used for single-cell phenotyping and spatial characterization of tissues; however, transparent methods are needed for comparing the performance of platforms, protocols and analytical pipelines. We developed a python software, jinxif, for reproducible image processing and utilize Jupyter notebooks to share our optimization of signal removal, antibody specificity, background correction and batch normalization of the multiplex imaging with a focus on cyclic immunofluorescence (CyCIF). Our work both improves the CyCIF methodology and provides a framework for multiplexed image analytics that can be easily shared and reproduced.


2021 ◽  
Author(s):  
Nadia M Huisjes ◽  
Thomas M Retzer ◽  
Matthias J Scherr ◽  
Rohit Agarwal ◽  
Barbara Safaric ◽  
...  

The rapid development of new imaging approaches is generating larger and more complex datasets revealing the time evolution of individual cells and biomolecules. Single-molecule techniques, in particular, provide access to rare intermediates in complex, multistage molecular pathways, but few standards exist for processing these information-rich datasets, posing challenges for wider dissemination. Here, we present Mars, an open-source platform for storage and processing of image-derived properties of biomolecules. Mars provides Fiji/ImageJ2 commands written in Java for common single-molecule analysis tasks using a Molecule Archive architecture that is easily adapted to complex, multistep analysis workflows. Three diverse workflows involving molecule tracking, multichannel fluorescence imaging, and force spectroscopy, demonstrate the range of analysis applications. A comprehensive graphical user interface written in JavaFX enhances biomolecule feature exploration by providing charting, tagging, region highlighting, scriptable dashboards, and interactive image views. The interoperability of ImageJ2 ensures Molecule Archives can easily be opened in multiple environments, including those written in Python using PyImageJ, for interactive scripting and visualization. Mars provides a flexible solution for reproducible analysis of image-derived properties facilitating the discovery and quantitative classification of new biological phenomena with an open data format accessible to everyone.


2021 ◽  
Author(s):  
Denis Schapiro ◽  
Artem Sokolov ◽  
Clarence Yapp ◽  
Yu-An Chen ◽  
Jeremy L. Muhlich ◽  
...  

AbstractHighly multiplexed tissue imaging makes detailed molecular analysis of single cells possible in a preserved spatial context. However, reproducible analysis of large multichannel images poses a substantial computational challenge. Here, we describe a modular and open-source computational pipeline, MCMICRO, for performing the sequential steps needed to transform whole-slide images into single-cell data. We demonstrate the use of MCMICRO on tissue and tumor images acquired using multiple imaging platforms, thereby providing a solid foundation for the continued development of tissue imaging software.


2021 ◽  
Vol 3 ◽  
Author(s):  
Julio Vega ◽  
Meng Li ◽  
Kwesi Aguillera ◽  
Nikunj Goel ◽  
Echhit Joshi ◽  
...  

Smartphone and wearable devices are widely used in behavioral and clinical research to collect longitudinal data that, along with ground truth data, are used to create models of human behavior. Mobile sensing researchers often program data processing and analysis code from scratch even though many research teams collect data from similar mobile sensors, platforms, and devices. This leads to significant inefficiency in not being able to replicate and build on others' work, inconsistency in quality of code and results, and lack of transparency when code is not shared alongside publications. We provide an overview of Reproducible Analysis Pipeline for Data Streams (RAPIDS), a reproducible pipeline to standardize the preprocessing, feature extraction, analysis, visualization, and reporting of data streams coming from mobile sensors. RAPIDS is formed by a group of R and Python scripts that are executed on top of reproducible virtual environments, orchestrated by a workflow management system, and organized following a consistent file structure for data science projects. We share open source, documented, extensible and tested code to preprocess, extract, and visualize behavioral features from data collected with any Android or iOS smartphone sensing app as well as Fitbit and Empatica wearable devices. RAPIDS allows researchers to process mobile sensor data in a rigorous and reproducible way. This saves time and effort during the data analysis phase of a project and facilitates sharing analysis workflows alongside publications.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gilles Maussion ◽  
Rhalena A. Thomas ◽  
Iveta Demirova ◽  
Gracia Gu ◽  
Eddie Cai ◽  
...  

AbstractQuantifying changes in DNA and RNA levels is essential in numerous molecular biology protocols. Quantitative real time PCR (qPCR) techniques have evolved to become commonplace, however, data analysis includes many time-consuming and cumbersome steps, which can lead to mistakes and misinterpretation of data. To address these bottlenecks, we have developed an open-source Python software to automate processing of result spreadsheets from qPCR machines, employing calculations usually performed manually. Auto-qPCR is a tool that saves time when computing qPCR data, helping to ensure reproducibility of qPCR experiment analyses. Our web-based app (https://auto-q-pcr.com/) is easy to use and does not require programming knowledge or software installation. Using Auto-qPCR, we provide examples of data treatment, display and statistical analyses for four different data processing modes within one program: (1) DNA quantification to identify genomic deletion or duplication events; (2) assessment of gene expression levels using an absolute model, and relative quantification (3) with or (4) without a reference sample. Our open access Auto-qPCR software saves the time of manual data analysis and provides a more systematic workflow, minimizing the risk of errors. Our program constitutes a new tool that can be incorporated into bioinformatic and molecular biology pipelines in clinical and research labs.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Ankur V Patel ◽  
Robert D Turner ◽  
Aline Rifflet ◽  
Adelina E Acosta-Martin ◽  
Andrew Nichols ◽  
...  

Many software solutions are available for proteomics and glycomics studies, but none are ideal for the structural analysis of peptidoglycan (PG), the essential and major component of bacterial cell envelopes. It icomprises glycan chains and peptide stems, both containing unusual amino acids and sugars. This has forced the field to rely on manual analysis approaches, which are time-consuming, labour-intensive, and prone to error. The lack of automated tools has hampered the ability to perform high-throughput analyses and prevented the adoption of a standard methodology. Here, we describe a novel tool called PGFinder for the analysis of PG structure and demonstrate that it represents a powerful tool to quantify PG fragments and discover novel structural features. Our analysis workflow, which relies on open-access tools, is a breakthrough towards a consistent and reproducible analysis of bacterial PGs. It represents a significant advance towards peptidoglycomics as a full-fledged discipline.


2021 ◽  
Vol 31 (12) ◽  
pp. 2150205
Author(s):  
Leonardo Ricci ◽  
Alessio Perinelli ◽  
Michele Castelluzzo ◽  
Stefano Euzzor ◽  
Riccardo Meucci

Detection of chaos in experimental data is a crucial issue in nonlinear science. Historically, one of the first evidences of a chaotic behavior in experimental recordings came from laser physics. In a recent work, a Minimal Universal Model of chaos was developed by revisiting the model of laser with feedback, and a first electronic implementation was discussed. Here, we propose an upgraded electronic implementation of the Minimal Universal Model, which allows for a precise and reproducible analysis of the model’s parameters space. As a marker of a possible chaotic behavior the variability of the spiking activity that characterizes one of the system’s coordinates was used. Relying on a numerical characterization of the relationship between spiking activity and maximum Lyapunov exponent at different parameter combinations, several potentially chaotic settings were selected. The analysis via divergence exponent method of experimental time series acquired by using those settings confirmed a robust chaotic behavior and provided values of the maximum Lyapunov exponent that are in very good agreement with the theoretical predictions. The results of this work further uphold the reliability of the Minimal Universal Model. In addition, the upgraded electronic implementation provides an easily controllable setup that allows for further developments aiming at coupling multiple chaotic systems and investigating synchronization processes.


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