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Shahraki, M. F.

Publications and source records attributed to Shahraki, M. F..

2 recordsLinked to original sources

Integrative chromatin state annotation of 234 human ENCODE4 cell types using Segway reveals disease drivers

Towards the goal of identifying functional elements in the human genome, the fourth and final phase of the ENCODE consortium has newly profiled hundreds of human tissues using sequencing-based measurements of genomic activity such as ChIP-seq measures of transcription factor binding and histone modification. Chromatin state annotations created by segmentation and genome annotation (SAGA) methods such as Segway have emerged as the predominant integrative summary of such epigenomic data sets. Here, we present the ENCODE4 catalog of Segway annotations, a set of sample-specific genome-wide Segway chromatin state annotations for 234 ENCODE human biosamples inferred from 1,794 functional genomics experiments. We define an updated vocabulary of chromatin state terms that includes patterns of activity present only in a subset of samples or identified only with rarely-performed assays. We show that these ENCODE4 Segway annotations accurately capture both general and cell-type-specific regulatory patterns, and do so with substantially improved sensitivity relative to prior large-scale chromatin annotation sets. This catalog facilitates the downstream discovery of regulatory mechanisms which underlie diseases and traits identified by genome-wide association studies.

genomics↗

TAXyl: An in-silico method for predicting the thermal activity for xylanases from GH10 and GH11 families

Growing industrial utilization of enzymes, and the increasing availability of metagenomic data highlights the demand for effective methods of targeted identification and verification of novel enzymes from various environmental microbiota. Xylanases are a class of enzymes with numerous industrial applications and are involved in the degradation of xylose, a component of lignocellulose. Optimum temperature of enzymes are essential factors to be considered when choosing appropriate biocatalysts for a particular purpose. Therefore, in-silico prediction of this attribute is a significant cost and time-effective step in the effort to characterize novel enzymes. The objective of this study was to develop a computational method to predict the thermal dependence of xylanases. This tool was then implemented for targeted screening of putative xylanases with specific thermal dependencies from metagenomic data and resulted in identification of three novel xylanases from sheep and cow rumen microbiota. Here we present TAXyl (Thermal Activity Prediction for Xylanase), a new sequence-based machine learning method that has been trained using a selected combination of various protein features. This random forest classifier discriminates non-thermophilic, thermophilic, and hyper-thermophilic xylanases. Models performance was evaluated through multiple iterations of six-fold cross-validations, and it exhibited a mean accuracy of [~]0.79. TAXyl is freely accessible as a web-service.

bioinformatics↗