BIO505T Final Term Objective Guess Paper 2023
- Type
- Final term past paper
- Course
- BIO505T Essentials of Genetics (Theory)
- Size
- PDF 632 KB
- Updated
- 23 Oct 2026
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- Double mutation has a fitter phenotype than either single mutation.
- Proteins are made of "amino acids"
- Nucleotides contain "ribose sugar"
- Sequence of development “haploid cells diploid zygote"
- Diploid number is obtained after "fertilization"
- Colichine produces "polyploidy"
- The uses of vntr "geomic mapping etc"
- RNA is obtained from"cytoplasm"
- Northern blot is used for *RNA analysis*.
- The following is not chromosomal aberration is *mitosis*.
- R banding has dark bands of *adenine and thymine content*.
- Cancer and infertility are the result of *genetic mutations*.
- Colchicine is used to *promote polyploidy*.
- A cross for determination of the genotype of an individual is called a *test cross*.
- Autosomal dominant diseases are caused by *dominant alleles on autosomal
- Mitochondrial DNA* is inherited through ovum, not sperm.
- Sequence difference compared to a reference standard present in at least 1-2% of a population is called *polymorphism*.
- Which on is sexual disease ____________________________Alzheimer's disease.
- Discontinuous variations are entirely genetically controlled.
- forward genetics is defined as____ The identification of genes responsible for a specific phenotype without prior knowledge of the gene's function.
- genetic marker for a single locus is _______ RFLP, Microsatellite, STS.
- in x-linked recessive trait all are true except__ "In X-linked recessive traits, males
can be carriers of the trait."/ it is present in females more than males
a healthy male and female have a sòn who is color blind .what is genetics of boy parents?
XcY
- Dark bands are those which contain fewer or less intense light waves, and light bands are those which contain more or more intense light waves.
- The chromosome number in an earthworm is 2.
likely genotypes of the boy's parents?
- Boy = XaY (got recessive allele from mother) He will be color blind.
- Position depended method of disease identification following _______Reverse
genetics
- Molecular biology, forensic , genes mapping are application of ________________VNTR
- Groups of human chromosomes are __________________________7
- Dna precipitation k liye konsa chemical use hota?___Isopropanol
- Important reagents for pcr. Option mai sb hi mojood thy tu _____ALL
- Mitochondrial inheritance ki cgaracteristics di thi option mai. Ghalat konsi ye btana tha. These are present chose other than these (⚫ Heteroplasy ⚫ Variable expression ⚫ Pleiotropy ⚫ Reduced penetrance ⚫Functional somatic mosaic).
- Q-PCR is commonly used to determine whether a DNA sequence is present in a sample and the number of its copies in the sample.
- Meiosis I ki characteristics pochi thi option mai. Ye b ALL
- In which pcr two pairs of primers are used.______Nested PCR
- In giemsa staining dark bands are rich in... A and T ans
- And light bands are rich in.... G and C ans
- During rna extraction, rna is extracted from the neucli of which cell. Rbc, wbc, or platelets
- Erythrocytes k bry mak 1 mcqs tha______ Erythrocytes (red blood cells) do not contain nuclei. They neither synthesize nor contain RNA.
- Which fur color of rabbit have highest numbers of genotypes. Grey
- Which genetic disorder have lowest frequency. Ans autosomal recessive disorder
- Which is an autosomal recessive disorder? (⚫ Bloom syndrome ⚫ Carpenter
syndrome ⚫ Cystic fibrosis ⚫ Thalasemia ⚫Many forms of mental retardation)
- Which mutation shortens the protein? Ans non-sense mutation
- How many cases of turner syndrome are due to ring chromosome. Ans 20%
- During inversion what is reversed.___chromosome sequence/segments of
- Which mutation suppreses the effect of other mutation. Ans suppresion mutation
- DOMINANT EPISTASIS: Epistatic gene exerts its affect with the presence of a dominant allele.
- Mutation that occur in regulatory region affects? Ans transcription, Translation
and splicing of protein
- AUTOSOMAL DOMINANT DISEASES (⚫ Marfan syndrome ⚫ Huntington's disease ⚫ Retinoblastoma ⚫Waardenburg syndrome ⚫Myotonic dystrophy ⚫ Polycystic kidney disease ⚫ Achondroplasia ⚫ Polydactyly ⚫ Heredity hearing loss)
- X-LINKED DOMINANT DISEASES: (⚫ Rett syndrome ⚫ Alport syndrome ⚫ Goltz syndrome ⚫ Fragile-X Syndrome)
- Homologous paired chromosomes have the same shape, size, and location of the centromere.
- in organic method of purification of DNA ...... IS USED TO remove protein (ans)
phenol chloroform
- ..... Is chelating agent(ans)EDTA
- ..... Result in two cells(ans) mitosis
- application thi VNTR ki uska answer bh VNTR hi th
- R banding has dark bands of: (ans) Heterochromatic
- Fur color in labrador retriever controlled by….(ans)2gene
- Two pairs of primer use in…(ans) nested PCR
probability that any son born will have pattern baldness?.. (ans)50%
- A mutation that are responsible for shorten of protein due to producing stop
codons….(ans)non sense mutation
- when allele of two gene segregate together and transmitted as a unit? What type of segregation occur... (Ans) Dependent segregation
- dna fingerprinting is an example of??VnTR
- If normal male and normal female are not color blind but their son is color blind what are the alleles of next generation: A) Son carry recessive allele
- Hemophilia is an example of____X linked chromosome.
- Two pairs of primer use in….. nested pcr
- Genes in drosophila.......13,700
- A mutation that are responsible for shorten of protein.......... Nonsense mutation
- ............. Caused frameshift mutation._______ Deletion
- First stage of mitosis.......Prophase
- First phase of mitosis........Prophase
- ............... is non-ionic buffer for DNA extraction ( cell lysis buffer)
- If both parents have heterozygous dominant disease, what will be the chance of a child not having that disease? (25%)
- microbiology, finger printing, genetic diversity and mapping of genomes are applications of........VNTR.
- Symbol of substitution ____ ">"
- RNA is genetic material in.....some viruses
- A type of genetic study in which , select a gene create a mutation then study its phenotype ............. Forward genetics.
- If two people who are both carrier for the genetically inherited fatal recessive disease decide to become parents , how many chances that their children will also be carriers.( 1
out of 4)
- Any change in nucleotide sequence of DNA gene is called......mutation
- Which disorder have the lowest frequency range.......X linked disorder.
- In phenol- chloroform DNA extraction lower organic phase contains........lipids
- DNA finger printing bioinformatics are applications of ( ans)VNTR
- R banding has dark bands of: ( ans) Heterochromatic
- Two pairs of primer use in…( ans) nested PCR
- A mutation that are responsible for shorten of protein due to producing stop codons….(
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