Yazar "Nisar, Haseeb" seçeneğine göre listele

Listeleniyor 1 - 3 / 3
  • Küçük Resim
    Öğe
    Correction to: Music of metagenomics—a review of its applications, analysis pipeline, and associated tools (Functional & Integrative Genomics, (2022), 22, 1, (3-26), 10.1007/s10142-021-00810-y)
    (Springer Science and Business Media Deutschland GmbH, 2022) Wajid, Bilal; Anwar, Faria; Wajid, Imran; Nisar, Haseeb; Meraj, Sharoze; Zafar, Ali; Al‑Shawaqfeh, Mustafa Kamal; Ekti, Ali Riza; Khatoon, Asia; Suchodolski, Jan S.
    The co-author Imran Wajid would like to update his second affiliation address to “School of Social Sciences, Istanbul Commerce University, Istanbul, Turkey”. The original article has been corrected.
  • Küçük Resim
    Öğe
    Music of metagenomics—a review of its applications, analysis pipeline, and associated tools
    (Springer, 2021) Wajid, Bilal; Anwar, Faria; Wajid, Imran; Nisar, Haseeb; Meraj, Sharoze; Zafar, Ali; Al‑Shawaqfeh, Mustafa Kamal; Ekti, Ali Rıza; Khatoon, Asia; Suchodolsk, Jan S.
    This humble efort highlights the intricate details of metagenomics in a simple, poetic, and rhythmic way. The paper enforces the signifcance of the research area, provides details about major analytical methods, examines the taxonomy and assembly of genomes, emphasizes some tools, and concludes by celebrating the richness of the ecosystem populated by the “metagenome.”
  • Küçük Resim
    Öğe
    Whole-genome sequencing as a first-tier diagnostic framework for rare genetic diseases
    (Sage, 2021) Nisar, Haseeb; Wajid, Bilal; Shahid, Samiah; Anwar, Faria; Wajid, Imran; Khatoon, Asia; Sattar, Mian Usman; Sadaf, Saima
    Rare diseases affect nearly 300 million people globally with most patients aged five or less. Traditional diagnostic approaches have provided much of the diagnosis; however, there are limitations. For instance, simply inadequate and untimely diagnosis adversely affects both the patient and their families. This review advocates the use of whole genome sequencing in clinical settings for diagnosis of rare genetic diseases by showcasing five case studies. These examples specifically describe the utilization of whole genome sequencing, which helped in providing relief to patients via correct diagnosis followed by use of precision medicine.