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Pop the Bird

Thesis Info

Author

Aamir Rashid

Supervisor

Hassan Khan

Department

Department of Computer Science

Program

BCS

Institute

COMSATS University Islamabad

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2015

Thesis Completion Status

Completed

Subject

Computer Science

Language

English

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676720019644

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اسلم عارف

اسلم عارف (۱۹۴۲ء۔پ) پسرور کے ایک گاؤں بن باجوہ میں پیدا ہوئے۔(۱۰۰۱) اپنے وقت کے نظم،غزل اور قطعات کے اچھے شاعر ہیں۔ ان کے قطعات میں جدت پائی جاتی ہے۔ چند قطعات ملاحظہ ہوں:

قبر کے پھول            

اے حسینہ سنوارلے گیسو

 

%اشک کب تک بہائے گی

 

3قبر کے پھول سوکھ جائیں گے

 

-زندگی لوٹ کر نہ آئے گی

 

â۱۰۰۲)

آخری انسان                            

ایک مفلس بندۂ مزدور پر روئے گا کون

 

زندگی میں بھی اگرچہ بے سرو سامان تھا

 

مر کے لیکن رہ گیا اس طرح بے گورو کفن

 

جیسے اس دنیا کا بس یہ آخری انسان تھا

 

۱۰۰۳)

 ۱۰۰۱۔رخشہ نسیم،’’سیالکوٹ میں اردو شاعری‘‘(بیسویں صدی کے دوران )ص:۳۲

۱۰۰۲۔ایضاً،ص:۳۳

۱۰۰۳۔ایضاً،ص:۳۴

 

امام طبری کا تفسیری منہج اور ترجیحات کا تحقیقی مطالعہ

The Jāmiʿ al-bayān ʿan taʾwīl āy al-Qurʾān (جامع البیان عن تاویل ای القران) the book of Quranic interpretation is known as Tafsīr al-Ṭabarī. The author Imām Ṭabarī was blessed for being skilled enough in presenting the message of Islam with different methods. The methodology he has chosen to explain the precious hidden beads of Holy Quran is associated with the methodology of tafsir bi-al-ma’thur (تفسیر بالماثور). His presented explanations are completely independent from the reflection of his personal opinions. The statements of the early stages of Islam, the direct transmissions by the Holy prophet Muhammad (ﷺ) and his companions were chiefly used to understand the meaning of Holy Quran. The jurisprudence, linguistic, and the philosophic approaches are also referred in his tafsir.

Development and Optimization of Polymerase Chain Reaction for Screening of Burkholderia Mallei Infection Among Indiginous Working Equines

Economically, Pakistan is an agricultural country as the agriculture sector offers employment to 42.3% of the country?s citizens involved with any kind of labor for their livelihood, 19.5% of its gross domestic product (GDP) comes from the agriculture sector apart from the raw materials for many other value-added sectors contributing to huge quantities of added indirect income; livestock sector as for instance, adding 58.33% to the worth of agriculture besides contributing 11.39% directly to GDP. Population of livestock are cattle 44.4, Buffalo 37.7, Sheep 30.1, goat 72.2, Camel 1.1, Horses 0.4, Asses 5.2, Mules 0.2 millions. Asses population increased from 4.9 to 5.2 million while population of Camel, Horses and mules remained unchanged since last year. Horses along with mules and donkeys facing many managerial, nutritional, noninfectious and infectious diseases which decreases production and performance, out of which infectious diseases such as Glanders is life threatening and pose zoonotic potential to human beings specially care takers, veterinarian and public health. To monitor threat due to these asymptomatic carriers to animals and human beings and from places having decreases frequency of disease Glanders in equines, it is unavoidable to develop and optimize a highly specific and sensitive molecular test such as PCR, required to decrease the number of results which are false negative and false positive findings besides being fast and accurate. 200 nasal and blood samples of working equines (horses, mules and donkeys) were collected from the Bahawalpur, Faisalabad, Gujranwala, Lahore and Multan at the sites of Brook hospital. All the samples were collected and transported to the WTO Quality Control Laboratory of UVAS, Lahore keeping in account the all microbiological hygienic and hazardous measures according to OIE protocols. All the animals were injected mallein PPD intra-dermally into the lower eyelid with the result noted after first and second day. Blood of animals were used for DNA extraction by commercially available DNA extraction kit. The extracted DNA were subjected to Gel Electrophoresis for integrity of the extracted DNA and then used further for amplification of target region of the DNA. The extracted DNA was used for the amplification of Flip IS407A gene region using the specific primers. Products of the PCR were visualized with UV light after electrophoresis of the gel and B. mallei was detected in only positive control. The study found high prevalence of the disease and existence of active nasal shedders in equines. The findings implicate importance of targeted surveillance in glanders suspected equines.