Results 121 to 130 of about 3,537,585 (186)

Investigating the paternal genetic structure and migration history of Chinese Qiang minority by Y-chromosome short tandem repeats. [PDF]

R Soc Open Sci
Fan GY, Zhu Y, Wang EN, Ju TG.
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Genome-wide detection of somatic mosaicism at short tandem repeats. [PDF]

Bioinformatics
Sehgal A, Ziaei Jam H, Shen A, Gymrek M.
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Microsatellite density landscapes illustrate short tandem repeats aggregation in the complete reference human genome. [PDF]

BMC Genomics
Xia Y, Li D, Chen T, Pan S, Huang H, Zhang W, Liang Y, Fu Y, Peng Z, Zhang H, Zhang L, Peng S, Shi R, He X, Zhou S, Jiao W, Zhao X, Wu X, Zhou L, Zhou J, Ouyang Q, Tian Y, Jiang X, Zhou Y, Tang S, Shen J, Ohshima K, Tan Z.   +27 more
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A detailed analysis of second and third-generation sequencing approaches for accurate length determination of short tandem repeats and homopolymers. [PDF]

Nucleic Acids Res
Jeanjean SI, Shen Y, Hardy LM, Daunay A, Delépine M, Gerber Z, Alberdi A, Tubacher E, Deleuze JF, How-Kit A.   +9 more
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Copy Number Variations in Short Tandem Repeats Modulate Growth Traits in Penaeid Shrimp Through Neighboring Gene Regulation. [PDF]

Animals (Basel)
Zhou H, Qiang G, Xia Y, Tan J, Fu Q, Luo K, Meng X, Chen B, Chen M, Sui J, Dai P, Li X, Liu M, Xing Q, Kong J, Luan S.   +15 more
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Short Tandem Repeats in the era of next-generation sequencing: from historical loci to population databases. [PDF]

Eur J Hum Genet
Uguen K, Michaud JL, Génin E.
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A machine learning approach for estimating Eastern Asian origins from massive screening of Y chromosomal short tandem repeats polymorphisms. [PDF]

Int J Legal Med
You H, Lee SD, Cho S.
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Clinal Variation in Short Tandem Repeats Linked to Gene Expression in Sunflower (<i>Helianthus annuus</i> L.). [PDF]

Biomolecules
Ranathunge C, Welch ME.
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Sequencing the orthologs of human autosomal forensic short tandem repeats provides individual- and species-level identification in African great apes. [PDF]

BMC Ecol Evol
Fedele E, Wetton JH, Jobling MA.
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Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriers. [PDF]

Brain Commun
Barbier M, Gareau T, Camuzat A, Guillaud-Bataille M, Boluda S, Clot F, Araktingi L, Borroni B, van der Zee J, Ghidoni R, Bellini S, Galimberti D, Rossi G, Nacmias B, De la Casa-Fages B, Pastor P, French Clinical and Genetic Research Network on FTD/FTD-ALS and PrevDemALS Study Groups , Latouche M, le Guern E, Durr A, Laquerrière A, Moccia R, Seilhean D, Alvarez V, Le Ber I.   +24 more
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