Red Blood Cell and Sickle Cell Detection from Microscopic Blood Images of Sickle Cell Anemic Patient

被引:0
|
作者
Patgiri, Chayashree [1 ]
Ganguly, Amrita [1 ]
机构
[1] Assam Engn Coll, Dept Elect Engn, Gauhati 13, India
来源
2019 INTERNATIONAL CONFERENCE ON WIRELESS COMMUNICATIONS, SIGNAL PROCESSING AND NETWORKING (WISPNET 2019): ADVANCING WIRELESS AND MOBILE COMMUNICATIONS TECHNOLOGIES FOR 2020 INFORMATION SOCIETY | 2019年
关键词
Sickle cell anemia (SCA); red blood cell; Niblack's thresholding; form factor;
D O I
10.1109/wispnet45539.2019.9032790
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Sickle cell anemia (SCA) is a type of haemolytic anemia which is the most commonly inherited blood disorder. Detection of red blood cell and sickle cell from sickle cell anemic person is a very challenging task. Besides traditional visual inspection of microscopic images, various methods have been developed which are based on image processing technique for faster and more accurate diagnosis of SCA. In this paper normal and abnormal red blood cells have been detected using Niblack's thresholding technique from microscopic blood images of sickle cell anemic patient. The process involves preprocessing of microscopic blood smear and segmenting the preprocessed image using Niblack's thresholding algorithm. Then using geometrical features of blood cells a metric (form factor) is calculated to classify normal red blood cells and abnormal cells.
引用
收藏
页码:474 / 478
页数:5
相关论文
共 50 条
  • [21] Red blood cell exchange in children with sickle cell disease
    Narcisse Elenga
    Vincent Vantilcke
    Elise Martin
    Emma Cuadro
    Pierre Selles
    Thierry Basset
    International Journal of Hematology, 2022, 115 : 107 - 113
  • [22] Red blood cell exchange in an emergency in sickle cell disease
    Hequet, O.
    Fort, R.
    Driss, F.
    TRANSFUSION AND APHERESIS SCIENCE, 2020, 59 (06)
  • [23] Therapeutic plasmapheresis and red blood cell exchange in a sickle cell trait patient with rhabdomyolysis
    Huang, Richard S. P.
    Tholpady, Ashok
    Wahed, Amer
    Chang, Brian
    Bai, Yu
    JOURNAL OF CLINICAL APHERESIS, 2012, 27 (06) : 342 - 345
  • [24] Red blood cell nitric oxide synthase modulates red blood cell deformability in sickle cell anemia
    Mozar, Anais
    Connes, Philippe
    Collins, Bianca
    Hardy-Dessources, Marie-Dominique
    Romana, Marc
    Lemonne, Nathalie
    Bloch, Wilhelm
    Grau, Marijke
    CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2016, 64 (01) : 47 - 53
  • [25] Reconsidering sickle cell trait testing of red blood cell units allocated to children with sickle cell disease
    Hajjaj, Omar, I
    Cserti-Gazdewich, Christine
    Dumevska, Letka
    Hanna, Mirette
    Lau, Wendy
    Lieberman, Lani
    Network, Canadian Obstetrical Pediatric Transfusion
    TRANSFUSION, 2023, 63 (03) : 507 - 514
  • [26] Red blood cell reduction of a sickle cell disease stem cell product
    Tanhehco, Yvette C.
    Delgado, Ana Catalina
    TRANSFUSION, 2021, 61 (11) : 3064 - 3065
  • [27] Sickle cell disease biochip: a functional red blood cell adhesion assay for monitoring sickle cell disease
    Alapan, Yunus
    Kim, Ceonne
    Adhikari, Anima
    Gray, Kayla E.
    Gurkan-Cavusoglu, Evren
    Little, Jane A.
    Gurkan, Umut A.
    TRANSLATIONAL RESEARCH, 2016, 173 : 74 - 91
  • [28] DETECTION OF BLOOD DONORS WITH SICKLE CELL TRAIT
    Diana Cristina, Martinez Millan
    Martinez Mabel, Ortiz de Salazar
    Richarte Angel, Gimenez
    Pons Patricia, Martinez
    Luis Roberto, Larrea Gonzalez
    Arbona Castano, Cristina
    HAEMATOLOGICA, 2016, 101 : 274 - 275
  • [29] Red blood cell alloimmunization in sickle cell disease patients in Uganda
    Natukunda, Bernard
    Schonewille, Henk
    Ndugwa, Christopher
    Brand, Anneke
    TRANSFUSION, 2010, 50 (01) : 20 - 25
  • [30] Heterogeneous Red Blood Cell Adhesion and Deformability in Sickle Cell Disease
    Alapan, Yunus
    Little, Jane A.
    Gurkan, Umut A.
    SCIENTIFIC REPORTS, 2014, 4