DeepMP – Detect DNA modifications in Nanopore Sequencing data

DeepMP

:: DESCRIPTION

DeepMP is a convolutional neural network (CNN)-based model that takes information from Nanopore signals and basecalling errors to detect whether a read is methylated or not.

::DEVELOPER

DeepMP team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  •  Linux
  • Python

:: DOWNLOAD

DeepMP

:: MORE INFORMATION

Citation:

Bonet J, Chen M, Dabad M, Heath S, Gonzalez-Perez A, Lopez-Bigas N, Lagergren J.
DeepMP: a deep learning tool to detect DNA base modifications on Nanopore sequencing data.
Bioinformatics. 2021 Oct 28:btab745. doi: 10.1093/bioinformatics/btab745. Epub ahead of print. PMID: 34718417.

CoSBI – Identify Combinatorial Chromatin Modification Patterns across Genomic Loci

CoSBI

:: DESCRIPTION

CoSBI (Coherent and Shifted Bicluster Identification) is a scalable subspace clustering algorithm  to identify the complete set of combinatorial chromatin modification patterns across the entire genome.

::DEVELOPER

Tan Laboratory

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 CoSBI

:: MORE INFORMATION

Citation:

Nucleic Acids Res. 2011 May;39(10):4063-75. doi: 10.1093/nar/gkr016. Epub 2011 Jan 25.
Combinatorial chromatin modification patterns in the human genome revealed by subspace clustering.
Ucar D1, Hu Q, Tan K.

histoneHMM 1.8 – Differential Analysis of Histone Modifications with broad Genomic Footprints

histoneHMM 1.8

:: DESCRIPTION

histoneHMM is a software to analyse ChIP-seq data of histone modifications with broad genomic footprints like H3K27me3. It allows for calling modified regions in single samples as well as for calling differentially modified regions in a comparison of two samples.

::DEVELOPER

histoneHMM team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • R

:: DOWNLOAD

 histoneHMM

:: MORE INFORMATION

Citation:

histoneHMM: Differential analysis of histone modifications with broad genomic footprints.
Heinig M, Colomé-Tatché M, Taudt A, Rintisch C, Schafer S, Pravenec M, Hubner N, Vingron M, Johannes F.
BMC Bioinformatics. 2015 Feb 22;16(1):60. doi: 10.1186/s12859-015-0491-6.

miRMOD 0.4 – miRNA Modification Identification tool

miRMOD 0.4

:: DESCRIPTION

miRMOD is the first windows based standalone GUI tool to identify and analyze non templated nucleotide additions and trimming at both the termini of the miRNA sequences in NGS data.

::DEVELOPER

Bioinformatics Centre ICGEB New Delhi

:: SCREENSHOTS

miRMOD

:: REQUIREMENTS

:: DOWNLOAD

 miRMOD

:: MORE INFORMATION

Citation

miRMOD: a tool for identification and analysis of 5′ and 3′ miRNA modifications in Next Generation Sequencing small RNA data.
Kaushik A, Saraf S, Mukherjee SK, Gupta D.
PeerJ. 2015 Oct 20;3:e1332.

dCMA – differential Chromatin Modification Analysis

dCMA

:: DESCRIPTION

dCMA is a package for identifying cell-type specific genomic regions with distinctive chromatin modifications.

::DEVELOPER

Shihua Zhang’s Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Windows/Linux
  • MatLab

:: DOWNLOAD

 dCMA

:: MORE INFORMATION

Citation

Nucleic Acids Res. 2013 Nov;41(20):9230-42. doi: 10.1093/nar/gkt712. Epub 2013 Aug 14.
Discovery of cell-type specific regulatory elements in the human genome using differential chromatin modification analysis.
Chen C1, Zhang S, Zhang XS.

HMCan 1.39 / HMCan-diff – Detection of (Differential) Chromatin Modifications in ChIP-seq data

HMCan 1.39 / HMCan-diff

:: DESCRIPTION

HMCan is Hidden Markov Model based tool that is developed to detect histone modification in cancer ChIP-seq data. It applies three correction steps to the data: copy number correction, GC bias correction and noise level correction.

HMCan-diff is a method designed specially to detect changes of histone modifications in ChIP-seq cancer samples or between a cancer sample and a normal control. HMCan-diff explicitly corrects for copy number bias as well as for other ChIP-seq technical biases such as GC-content and mappability biases, and variable levels of signal-to-noise in different samples. HMCan-diff uses a three state hidden Markov model to detect regions of differential histone modifications.

::DEVELOPER

Boeva lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 HMCan , HMCan-diff

:: MORE INFORMATION

Citation

Ashoor H, Louis-Brennetot C, Janoueix-Lerosey I, Bajic VB, Boeva V.
HMCan-diff: a method to detect changes in histone modifications in cells with different genetic characteristics.
Nucleic Acids Res. 2017 May 5;45(8):e58. doi: 10.1093/nar/gkw1319. PMID: 28053124; PMCID: PMC5416852.

Bioinformatics. 2013 Dec 1;29(23):2979-86. doi: 10.1093/bioinformatics/btt524. Epub 2013 Sep 9.
HMCan: a method for detecting chromatin modifications in cancer samples using ChIP-seq data.
Ashoor H1, Hérault A, Kamoun A, Radvanyi F, Bajic VB, Barillot E, Boeva V.

jEcho 1.0C – An Evolved Weight Vector to CHaracterize the protein’s post-translational Modification mOtifs

jEcho 1.0C

:: DESCRIPTION

jEcho is an Evolved weight vector to CHaracterize the protein’s posttranslational modification mOtifs.

::DEVELOPER

Health Informatics Lab (HILab)

:: SCREENSHOTS

:: REQUIREMENTS

  • Linux/ MacOsX/ Windows
  • Java

:: DOWNLOAD

 jEcho

:: MORE INFORMATION

Citation

Interdiscip Sci. 2015 Jun;7(2):194-9. doi: 10.1007/s12539-015-0260-2. Epub 2015 Aug 6.
jEcho: an Evolved weight vector to CHaracterize the protein’s posttranslational modification mOtifs.
Zhao M, Zhang Z, Mai G, Luo Y, Zhou F.

iRNA-PseColl – Identifying Occurrence Sites of different RNA Modifications

iRNA-PseColl

:: DESCRIPTION

iRNA-PseColl is seamless platform for identifying the occurrence sites of different RNA modifications by incorporating collective effects of nucleotides into PseKNC

::DEVELOPER

LinDing Group

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

 NO

:: MORE INFORMATION

Citation

iRNA-PseColl: Identifying the Occurrence Sites of Different RNA Modifications by Incorporating Collective Effects of Nucleotides into PseKNC.
Feng P, Ding H, Yang H, Chen W, Lin H, Chou KC.
Mol Ther Nucleic Acids. 2017 Jun 16;7:155-163. doi: 10.1016/j.omtn.2017.03.006.

iRNA-3typeA – Identifying 3-types of Modification at RNA’s Adenosine Sites

iRNA-3typeA

:: DESCRIPTION

iRNA-3typeA web-server allows for simultaneously identifying the most frequently observed N1-methyladenosine (m1A), N6-methyladenosine (m6A) and adenosine to inosine (A-to-I) modifications in both H. sapiens and M. musculus transcriptomes.

::DEVELOPER

LinDing Group

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

 NO

:: MORE INFORMATION

Citation

iRNA-3typeA: Identifying Three Types of Modification at RNA’s Adenosine Sites.
Chen W, Feng P, Yang H, Ding H, Lin H, Chou KC.
Mol Ther Nucleic Acids. 2018 Jun 1;11:468-474. doi: 10.1016/j.omtn.2018.03.012.

tRNAmod – Prediciton of tRNA Modifications

tRNAmod

:: DESCRIPTION

The tRNAmod is a web-server for the prediction of transfer RNA (tRNA) modifications. Post-transcriptional modifications of tRNA plays a major role in their functionality. It provides both flexibility as well as rigidity and fine tune tRNA structure for the maximum performance.

::DEVELOPER

tRNAmod team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

 NO

:: MORE INFORMATION

Citation

Prediction of uridine modifications in tRNA sequences.
Panwar B, Raghava GP.
BMC Bioinformatics. 2014 Oct 2;15:326. doi: 10.1186/1471-2105-15-326.

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