The influence of process parameters on the impact resistance of 3D printed PLA specimens under water-absorption and heat-treated conditions von Kumar Mishra, Pradeep, Ponnusamy, Senthil, Reddy Nallamilli, Mohan Satyanarayana

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Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutio... von Chaubey, Alka, Shenoy, Suresh, Mathur, Abhinav, Ma, Zeqiang, Valencia, C Alexander, Reddy Nallamilli, Babi R, Szekeres, Jr, Edward, Stansberry, Leah, Liu, Ruby, Hegde, Madhuri R

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Effect of long-term embryo cryopreservation on subsequent frozen embryo transfer outcomes: A retrospective cohort study von Reddy, Nallamilli, Parimala, Chinta, Karuppusami, Reka, Mangalraj, Ann, Kunjummen, Aleyamma

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Osteoporosis Detection Using Deep Learning on X-Ray images of Human Spine von Mane, Pallavi R, Vemulapalli, Jaswant, Reddy, Nallamilli Srikar, Anudeep, Nelanutala, Prabhu, Ghanashyama

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P599: Beyond single nucleotide variants and copy number variations: Spinal muscular atrophy and repeat expansion disorders screening by whole genome sequencing von Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Hegde, Madhuri

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Role of hysterosalpingography in diagnosing tubal blockage - A prospective diagnostic study von Antonisamy, Nikita, Reddy, Nallamilli, Chinta, Parimala, Waanbah, Batiston, Samadhiya, Richa, Aleyamma, T, Antonisamy, Belavendra, Kamath, Mohan

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P643: Unveiling noncoding DMD variants: Synergizing RNA sequencing and DNA sequencing for enhanced molecular diagnosis von Pan, Yinghong, Guo, Fen, Ma, Zeqiang, Reddy Nallamilli, Babi Ramesh, Liu, Ruby, Quirin, Kayla, Martin, Ann, Hegde, Madhuri

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P638: Genomic breakpoint analysis facilitates identification of complex rearrangements and re-classification of non-tandem duplications in the DMD gene von Guruju, Naga, Jump, Vanessa, Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Steigerwalt, Jill, Collins, Christin, Bean, Lora, Hegde, Madhuri

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Thoracolumbar Sacral Orthosis for Spinal Fractures: What's the Evidence and Do Patients Use Them? von Mehta, Sonu, Yusuf, Baasil S, Chiew, Daphne, Rathore, Sameer, Reddy, Nallamilli R, Nair, Deepak, Mahajan, Uday, Madhusudhan, Thayur R, Vedamurthy, Adhiyaman

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P502: How does multiomics help variant reclassification? von Liu, Ruby, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Guruju, Naga, Hegde, Madhuri

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Global analysis of lysine acetylation suggests the involvement of protein acetylation in diverse biological processes in rice (Oryza sativa) von Nallamilli, Babi Ramesh Reddy, Edelmann, Mariola J, Zhong, Xiaoxian, Tan, Feng, Mujahid, Hana, Zhang, Jian, Nanduri, Bindu, Peng, Zhaohua

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Polycomb group gene OsFIE2 regulates rice (Oryza sativa) seed development and grain filling via a mechanism distinct from Arabidopsis von Nallamilli, Babi Ramesh Reddy, Zhang, Jian, Mujahid, Hana, Malone, Brandon M, Bridges, Susan M, Peng, Zhaohua

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P714: Genome screening of newborns: Sequencing is easy, assessing the clinical utility of genomic findings uncovered in asymptomatic children is challenging von Balciuniene, Jorune, Liu, Ruby, Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Eprem, Mathur, Abhinav, Ma, Zeqiang, Carmichael, Jonathan, Collins, Christin, da Silva, Cristina, Kirmse, Brian, Bleyl, Steven, Hegde, Madhuri

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Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients von Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Tanner, Alice, Ankala, Arunkanth, Schneider, Thomas, da Silva, Cristina, Beadling, Randall, Alexander, John J., Askree, Syed Hussain, Whitt, Zachary, Bean, Lora, Collins, Christin, Khadilkar, Satish, Gaitonde, Pradnya, Dastur, Rashna, Wicklund, Matthew, Mozaffar, Tahseen, Harms, Matthew, Rufibach, Laura, Mittal, Plavi, Hegde, Madhuri

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Molecular Diagnosis of Duchenne Muscular Dystrophy von Nallamilli, Babi Ramesh Reddy, Ankala, Arunkanth, Hegde, Madhuri

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P389: Real-world evidence demonstrating why genome sequencing should be recommended as the first-tier genetic test von Guo, Fen, Liu, Ruby, Pan, Yinghong, Collins, Christin D., Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Balciuniene, Jorune, Hegde, Madhuri

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P425: Unparalleled power of genome sequencing in screening ostensibly healthy newborns and children: Findings from the first real-world dataset von Balciuniene, Jorune, Liu, Ruby, Collins, Christin, Bean, Lora, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Hegde, Madhuri

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P426: Recognizing the promise and potential pitfalls of genomic medicine through routine rapid whole genome sequencing von Bean, Lora, Collins, Christin, Guo, Fen, Balciuniene, Jorune, Chen-Deutsch, Xiangwen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Yousaf, Rizwan, Fura, Kristina, Woodman, Amber, Liu, Ruby, Zhang, Jenny, Liebmann, Kate, Gerow, Julia, Chin, Ephrem, Hegde, Madhuri

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Breakpoint spanning PCR of the DMD gene to resolve discrepancy between MLPA and targeted aCGH results to confirm predicted effect on reading frame von Ulm, E, Hegde, M, Ramesh Reddy Nallamilli, B, Alexander, J, Wong, B

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Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent von Chakravorty, Samya, Nallamilli, Babi Ramesh Reddy, Khadilkar, Satish Vasant, Singla, Madhu Bala, Bhutada, Ashish, Dastur, Rashna, Gaitonde, Pradnya Satish, Rufibach, Laura E, Gloster, Logan, Hegde, Madhuri

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