scholarly journals The first mitochondrial genome data of an old world fruit bat, Cynopterus sphinx from Malaysia

2021 ◽  
Vol 6 (1) ◽  
pp. 53-55
Author(s):  
Puteri Nur Syahzanani Jahari ◽  
Shahfiz Mohd Azman ◽  
Kaviarasu Munian ◽  
Nur Alwani Zakaria ◽  
Mohd Shahir Shamsir Omar ◽  
...  
2010 ◽  
Vol 1352 ◽  
pp. 108-117 ◽  
Author(s):  
Ambigapathy Ganesh ◽  
Wieslaw Bogdanowicz ◽  
Moritz Haupt ◽  
Ganapathy Marimuthu ◽  
Koilmani Emmanuvel Rajan

2004 ◽  
Vol 33 (2) ◽  
pp. 321-332 ◽  
Author(s):  
Iñaki Ruiz-Trillo ◽  
Marta Riutort ◽  
H. Matthew Fourcade ◽  
Jaume Baguñà ◽  
Jeffrey L. Boore

2021 ◽  
Vol 23 (1) ◽  
Author(s):  
Anbalagan Rathinakumar ◽  
Murugavel Baheerathan ◽  
Barbara A. Caspers ◽  
Joseph J. Erinjery ◽  
Perumalswamy Kaliraj ◽  
...  

2020 ◽  
Vol 36 (20) ◽  
pp. 5115-5116 ◽  
Author(s):  
August E Woerner ◽  
Jennifer Churchill Cihlar ◽  
Utpal Smart ◽  
Bruce Budowle

Abstract Motivation Assays in mitochondrial genomics rely on accurate read mapping and variant calling. However, there are known and unknown nuclear paralogs that have fundamentally different genetic properties than that of the mitochondrial genome. Such paralogs complicate the interpretation of mitochondrial genome data and confound variant calling. Results Remove the Numts! (RtN!) was developed to categorize reads from massively parallel sequencing data not based on the expected properties and sequence identities of paralogous nuclear encoded mitochondrial sequences, but instead using sequence similarity to a large database of publicly available mitochondrial genomes. RtN! removes low-level sequencing noise and mitochondrial paralogs while not impacting variant calling, while competing methods were shown to remove true variants from mitochondrial mixtures. Availability and implementation https://github.com/Ahhgust/RtN Supplementary information Supplementary data are available at Bioinformatics online.


2019 ◽  
Vol 13 (S1) ◽  
Author(s):  
Rongjie Wang ◽  
Tianyi Zang ◽  
Yadong Wang

Abstract Background In recent years, with the development of high-throughput genome sequencing technologies, a large amount of genome data has been generated, which has caused widespread concern about data storage and transmission costs. However, how to effectively compression genome sequences data remains an unsolved problem. Results In this paper, we propose a compression method using machine learning techniques (DeepDNA), for compressing human mitochondrial genome data. The experimental results show the effectiveness of our proposed method compared with other on the human mitochondrial genome data. Conclusions The compression method we proposed can be classified as non-reference based method, but the compression effect is comparable to that of reference based methods. Moreover, our method not only have a well compression results in the population genome with large redundancy, but also in the single genome with small redundancy. The codes of DeepDNA are available at https://github.com/rongjiewang/DeepDNA.


2019 ◽  
Vol 7 (1) ◽  
pp. 721-723 ◽  
Author(s):  
Charla Marshall ◽  
Kimberly Sturk-Andreaggi ◽  
Joseph D. Ring ◽  
Cassandra R. Taylor ◽  
Suzanne Barritt-Ross ◽  
...  

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